Remedy Labs

Lidocaine Base BP – Active Pharmaceutical Ingredient (API)
Product Name: Lidocaine Base BPOther Names: Lignocaine Base, Xylocaine BaseCAS Number: 137-58-6 Molecular Formula: C₁₄H₂₂N₂O Molecular Weight: 234.34 g/mol Pharmacopoeial Standard: British Pharmacopoeia (BP) – Pharmaceutical GradeAppearance: White to off-white crystalline powder Purity (Assay): ≥99% (Typical)Grade: BP / USP / EP / IP (as per customer requirement)Packaging: 25 kg HDPE drum / Fiber drum – export quality.

Description:
Lidocaine Base BP is a high-quality active pharmaceutical ingredient (API) manufactured to meet stringent British Pharmacopoeia (BP) standards for pharmaceutical use. It is an amide-type local anesthetic widely used as a raw material in the production of anesthetic formulations. Lidocaine works by blocking voltage-gated sodium channels on nerve cells, inhibiting nerve impulse transmission to provide effective local or regional anesthesia. This BP grade API is suitable for pharmaceutical manufacturing where compliance with British Pharmacopoeia specifications is required for regulatory approval and quality assurance. High-purity and consistent quality make it ideal for use in both domestic and export markets.
Key Features & Benefits:BP-Certified API — Conforms to British Pharmacopoeia standards for identity, purity, and quality.High Purity & Consistency — Ensures reproducible performance in finished formulations.Versatile Use — Suitable for topical, injectable, and other dosage form formulations.Reliable Raw Material — Ideal for manufacturing local anesthetic products such as creams, gels, ointments, sprays, and injectables.Pharma-Grade Quality — Meets international pharmacopeial standards (BP, USP, EP, IP).Export-Ready Packaging — Secure packaging to maintain product integrity during transit.
Applications:Local anesthetics for medical, dental, and surgical procedures.API in topical analgesic formulations (creams, gels, sprays).Intermediate in pharmaceutical synthesis and industrial production.Used in products requiring BP-compliant raw materials for regulatory approval.
Storage & Handling:Store in a cool, dry, well-ventilated area away from heat, moisture, and direct sunlight. Keep containers tightly closed when not in use to preserve product stability and prevent contamination.

Benzocaine API Powder – Pharmaceutical Grade
Product Name: Benzocaine API Powder.Chemical Name: Ethyl 4-aminobenzoate.CAS Number: 94-09-7Molecular Formula: C₉H₁₁NO₂Appearance: White to off-white crystalline powder.Grade: Pharmaceutical / USP/BP standard.Purity: ≥ 99.0% (or as per customer requirement)

Description:

Benzocaine API Powder is a high-quality active pharmaceutical ingredient widely used in the formulation of topical local anesthetic products. It provides rapid and effective temporary pain relief by blocking peripheral nerve signals, making it ideal for use in dental gels, throat lozenges, sprays, ointments, and other pain relief formulations.
Key Features:High purity meeting pharmacopeial standards (USP/BP).Fine, consistent particle size for easy formulation.Stable, free-flowing powder suitable for bulk processing.Excellent compatibility with excipients and  solvents.
Reliable quality with Certificate of Analysis (COA).
Applications:Topical analgesic and anesthetic formulations.Dental and oral care gels, lozenges, and sprays.OTC pain relief products.Pharmaceutical manufacturing and contract formulation.
Packaging & Storage:Available in 1 kg, 5 kg, 25 kg drum or customized packing.Store in a cool, dry place, away from direct sunlight.Shelf life: Standard 2–3 years under recommended conditions.

Tadalafil Citrate API – Product Description
Product Name: Tadalafil Citrate APICAS No.: 171596-29-5 (for tadalafil citrate)Chemical Name: Tadalafil citrate (salt form of tadalafil)Molecular Formula: C₂₂H₁₉N₃O₄•C₆H₈O₇ (approx.)Purity: ≥99% (or as per customer requirement)Appearance: White to Off-White PowderCategory: Pharmaceutical Active Pharmaceutical Ingredient (API)

Product Overview:
Tadalafil Citrate API is a high-quality pharmaceutical intermediary used in the manufacture of therapeutic formulations. It is the citrate salt form of tadalafil, a long-acting phosphodiesterase type 5 (PDE5) inhibitor widely used in the treatment of erectile dysfunction and related indications. This API grade material is suitable for bulk drug manufacturing, formulation development, and pharmaceutical production.
Key Features & Benefits:Excellent Purity: High-grade API with consistent quality and performance.Pharmaceutical-Grade: Manufactured under stringent quality standards for drug formulation use.Formulation-Ready: Compatible with tablets, capsules, and oral solid dosage forms.Stable & Reliable: Good chemical stability and controlled impurity profile.Batch Consistency: Uniform quality across production batches.
Packaging Options:1 kg, 5 kg, 10 kg HDPE Bags with Inner PE Liner.25 kg / Customized packaging available on request.
Storage & Handling:Store in a cool, dry, and well-ventilated place.Keep the container tightly closed.Avoid exposure to moisture and direct sunlight.Handle according to standard pharmaceutical safety practices.
Why Choose Us:Trusted API supplier with global export experience.Competitive pricing with flexible Minimum Order Quantities (MOQ).Prompt delivery and responsive customer support.Technical assistance and tailored solutions available. 

Tadalafil USP API Powder – Pharmaceutical Grade
Product Name: Tadalafil USP APIChemical Name: (6R,12aR)-6-(1,3-Benzodioxol-5-yl)-2-methyl-2,3,6,7,12,12a-hexahydropyrazino[1′,2′:1,6]pyrido[3,4-b]indole-1,4-dioneCAS Number: 171596-29-5 Molecular Formula: C₂₂H₁₉N₃O₄ Molecular Weight: ~389.4 g/mol Appearance: White to off-white crystalline powder Grade: Pharmaceutical / USP Standard Purity: ≥ 99.0% (or as per customer specification)

Description:
Tadalafil USP API Powder is a high-quality active pharmaceutical ingredient used in the manufacture of pharmaceutical formulations for treating erectile dysfunction (ED), benign prostatic hyperplasia (BPH), and pulmonary arterial hypertension (in specific formulations). It belongs to the class of phosphodiesterase type 5 (PDE5) inhibitors, acting to increase blood flow by relaxing vascular smooth muscle tissue. 
Key Features & Benefits:USP (United States Pharmacopeia) grade pharmaceutical-quality API.High purity with stringent quality testing and Certificate of Analysis (COA). White to off-white crystalline powder — ideal for formulation and processing. Stable and consistent batch-to-batch quality for reliable manufacturing.Compatible with a variety of excipients and further formulation processes. Manufactured under strict quality systems (cGMP compliance optional). 
Physical & Chemical Properties:Solubility: Practically insoluble in water; soluble in certain organic solvents (e.g., methanol, ethanol). Melting Point: ~298–303°C Assay: ≥99% by HPLC (typical) 
Packaging & Storage:Standard Packaging: 1 kg / 5 kg / 25 kg drums or customized packing.Storage: Store in a cool, dry place, protected from moisture and direct sunlight.Shelf Life: Typically 2–5 years under recommended conditions. 

Hyoscine Butyl Bromide BP
Product Name:Hyoscine Butyl Bromide BPSynonyms: Butylscopolamine Bromide, N-Butylscopolammonium BromideCAS No.: 149-64-4.Grade: BP / IP / USP (Pharmaceutical-grade API).

Product Description:
Hyoscine Butyl Bromide BP is a high-quality active pharmaceutical ingredient (API) commonly used in the manufacture of antispasmodic medicines indicated for the relief of smooth muscle spasms of the gastrointestinal and genitourinary tracts. It is a quaternary ammonium anticholinergic agent that works by blocking the action of acetylcholine on muscarinic receptors, helping to relax smooth muscles and alleviate discomfort associated with cramps and spasms.
Chemical & Physical Properties:Chemical Name: Hyoscine (as butylbromide).Molecular Formula: C₁₁H₃₀BrNO₄.Molecular Weight: ~440.37 g/mol.Appearance: White to off-white crystalline powder. Purity: Typically meets BP/IP/USP. Solubility: Freely soluble in water, slightly soluble in alcohols. Melting Point: ~137–141 °C.
Key Features & Benefits:Pharmaceutical-grade API suitable for finished dosage formulations such as tablets, injections, and oral liquids.Consistent quality & purity meeting BP/IP/USP specifications.Effective antispasmodic action through peripheral muscarinic receptor inhibition. Stable crystalline powder ideal for handling and formulation.
Usage & Handling:For pharmaceutical manufacturing and research use only (not for direct consumption).Store in a cool, dry, and well-ventilated area, protected from moisture and direct sunlight.Follow all regulatory, safety, and compliance standards during handling and storage.

Cetirizine Dihydrochloride USP API Powder – Pharmaceutical Grade
Product Name: Cetirizine Dihydrochloride USP APIChemical Name: 2-[2-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]ethoxy]acetic acid dihydrochlorideCAS Number: 83881-52-1 Molecular Formula: C₂₁H₂₅ClN₂O₃·2HCl Molecular Weight: 461.82 g/mol Appearance: White to off-white crystalline powder Grade: USP / IP / BP / EP pharmaceutical standard Purity: ≥ 99% (pharmaceutical grade)

Description:
Cetirizine Dihydrochloride USP API Powder is a high-purity active pharmaceutical ingredient (API) used in the formulation of antihistamine and anti-allergic medications. It belongs to the second-generation H1 receptor antihistamines, designed to relieve symptoms associated with allergic rhinitis, hay fever, chronic urticaria (hives), and other allergic conditions with minimal sedation.
Key Features & Benefits:Pharmaceutical-grade quality meeting USP/EP/BP/IP standards.High purity ≥99% ensuring consistent performance for formulation.White to off-white crystalline powder, easy to handle and process.Freely soluble in water and suitable solvents for diverse APIs .Reliable batch-to-batch quality with Certificate of Analysis (COA).Ideal for oral solid dosage and liquid formulations.
Physical & Chemical Properties:Appearance: White to off-white crystalline powder.Solubility: Freely soluble in water and methanol.Melting Point: Approx. 225–230 °C (varies by source).Assay (HPLC): ≥ 99% pharmaceutical grade.
Packaging & Storage:Standard Packaging: 1 kg, 5 kg, 25 kg drums (custom options available).Storage: Store in a cool, dry place, protected from moisture and direct sunlight.Shelf Life: Typically 2–5 years under recommended conditions.

Hyoscine Butyl Bromide API
Product Name: Hyoscine Butyl Bromide APICAS No.: 149-64-4.Synonyms:• Hyoscine N-butyl bromide• N-Butylscopolamine bromide• Scopolamine butylbromide• Butylscopolamine bromideMolecular Formula: C₂₁H₃₀BrNO₄.Molecular Weight: ~440.37 g/mol. ([turn0search1], [turn0search8]).

Product Overview:
Hyoscine Butyl Bromide API is a pharmaceutical-grade active pharmaceutical ingredient widely used in the formulation of antispasmodic and smooth muscle relaxant medications. It is supplied as a white to off-white crystalline powder with consistent purity and quality that meets global pharmacopeial standards (IP/BP/USP). This API serves as a key functional ingredient for treating smooth muscle cramps associated with gastrointestinal and genitourinary tracts. 
Key Specifications:Appearance: White to off-white crystalline powder. Assay/Purity: High pharmaceutical-grade (typically ≥ 98 % depending on spec). CAS Number: 149-64-4. Grade: IP / BP / USP as required. Form: Powder. Packaging: 25 kg HDPE/fiber drums or as per customer requirement. Storage: Store in a cool, dry place in airtight containers, protected from light and moisture.
Product Features:Pharmaceutical-Grade API: Manufactured to meet regulatory standards for drug production. Consistent Quality: Superior purity and stability for reliable formulation performance. Documentation Support: Supplied with COA, MSDS, and test reports. Ideal for Bulk Use: Suitable for pharmaceutical manufacturers, contract formulators, and exporters.
Applications:Hyoscine Butyl Bromide API is primarily used as a core ingredient in the pharmaceutical industry for:Antispasmodic Formulations: Used in tablets, capsules, and liquid preparations to relieve smooth muscle spasms in the GI and urinary tracts. Gastrointestinal Therapeutics: Helps alleviate abdominal cramps, irritable bowel symptoms, biliary colic and renal colic by relaxing smooth muscles. Pre-Procedural Use: Employed in drugs that reduce muscle movement during procedures like imaging or endoscopy. Muscle Relaxation Products: Can be used in combination formulations targeting menstrual cramps and other smooth muscle conditions.
Handling & Storage:Store Hyoscine Butyl Bromide API in a cool, dry, and well-ventilated place, keeping it in airtight containers away from moisture and sunlight. Use appropriate PPE when handling the API to maintain product integrity.
Why Choose Our Hyoscine Butyl Bromide API:Reliable Purity & Performance: Suitable for high-quality pharmaceutical products.Global Compliance: Meets IP/BP/USP standards with complete documentation.Bulk Supply & Support: Flexible packaging options and export-ready supply.Trusted Quality: Ideal for contract manufacturers and API distributors.

Lidocaine Hydrochloride EP
Product Name: Lidocaine Hydrochloride BP / EPSynonyms: Lignocaine Hydrochloride BP/EP, Lidocaine HCl Monohydrate, Xylocaine HydrochlorideChemical Name: 2‑(Diethylamino)‑N‑(2,6‑dimethylphenyl)acetamide Hydrochloride MonohydrateCAS No.: 6108‑05‑0 (monohydrate) / 73‑78‑9 (anhydrous form) Molecular Formula: C₁₄H₂₂N₂O·HCl·H₂O Molecular Weight: ~288.8 g/mol Appearance: White to off‑white crystalline powder Grade: Pharmacopoeial BP / EP API (British and European Pharmacopeia compliant).

Product Description:
Lidocaine Hydrochloride BP / EP is a high‑purity active pharmaceutical ingredient (API) supplied as a fine white to off‑white crystalline powder, manufactured under stringent quality standards to meet British Pharmacopoeia (BP) and European Pharmacopoeia (EP) specifications. It is highly soluble in water and freely soluble in ethanol, making it suitable for a wide range of medical and pharmaceutical formulations. Lidocaine Hydrochloride is the hydrochloride salt of lidocaine, a well‑established local anesthetic agent with rapid onset and intermediate duration of action. It functions by blocking sodium ion channels in nerve cells, thereby inhibiting nerve impulse transmission and providing effective local or regional anesthesia. Lidocaine HCl also exhibits class IB antiarrhythmic activity for certain cardiac uses under clinical supervision.
Key Features:BP / EP Pharmacopeial Quality: Conforms to stringent British and European pharmacopoeial standards for identity, purity and assay. High Purity API: Typically meets assay criteria (~99.0 – 101.0 % anhydrous basis) as per EP monograph. White / Off‑white Powder: Easy to handle, process and formulate. Excellent Solubility: Very soluble in water; freely soluble in ethanol — ideal for injections, gels, creams or solutions. Versatile Applications: Suitable for local anesthetic products and antiarrhythmic formulations. Consistent Quality: Produced with rigorous quality control and documentation (COA, MSDS).
Typical Pharmaceutical Applications:Local Anesthetic Formulations: Injectable solutions for dental, surgical or minor procedures. Topical Preparations: Gels, creams, sprays and ointments for pain relief. Antiarrhythmic Products: Component in cardiac care under appropriate medical use. Pharmaceutical Manufacturing: Raw material API for finished dosage forms.
Typical Physical & Chemical Properties:Appearance: White to off‑white crystalline powder. Solubility: Very soluble in water; freely soluble in ethanol. Melting Range: ~74 – 79 °C (monohydrate). Assay Range (EP): ~99.0 – 101.0 % (anhydrous basis).
Packaging & Storage:Offered in 25 kg HDPE or fiber drums with protective liners or customized pharma packaging per buyer requirements. Store in a cool, dry, and shaded place away from moisture and direct sunlight to preserve stability.

Fluconazole API Powder
Product Name: Fluconazole API PowderCAS No.: 86386‑73‑4Synonyms: Diflucan, Difluconazole, TriflucanGrade: IP / BP / USP / Pharma‑Grade Active Pharmaceutical Ingredient.

Product Overview:

Fluconazole API Powder is a high‑quality active pharmaceutical ingredient (API) belonging to the triazole antifungal class. It is widely used in the pharmaceutical industry as the key raw material for manufacturing antifungal medicines that treat a broad range of systemic and superficial fungal infections. Fluconazole works by inhibiting the 14α‑demethylase enzyme, which disrupts the synthesis of ergosterol—a critical component of the fungal cell membrane—thereby weakening the membrane and inhibiting fungal growth.
Chemical & Physical Properties:Chemical Name: 2‑(2,4‑Difluorophenyl)‑1,3‑bis(1H‑1,2,4‑triazol‑1‑yl)propan‑2‑ol. Molecular Formula: C₁₃H₁₂F₂N₆O. Molecular Weight: ≈ 306.27 g/mol.Appearance: White to off‑white crystalline powder. Purity: Typically ≥ 98–99 % (pharmacopeial standard). Solubility: Slightly soluble in water; soluble in many organic solvents such as methanol and acetone. Melting Point: ~138–140 °C.
Key Features & Benefits:Pharmaceutical‑grade API compliant with global standards such as IP / BP / USP (with COA & MSDS available on request). Broad‑spectrum antifungal activity effective against Candida species, Cryptococcus species, and other fungal pathogens. Stable crystalline powder form for ease of handling, storage, and formulation. High assay and consistent quality for reliable pharmaceutical production. Suitable for both oral and systemic antifungal formulations including tablets, capsules, and injectables.Usage & Handling:For pharmaceutical manufacturing and R&D use only (not for direct human consumption).Store in a cool, dry, ventilated place protected from moisture, heat, and direct light. Use appropriate PPE (gloves, goggles, masks) during handling.Follow all regulatory, safety, and compliance standards for APIs.

Domperidone API Powder
Product Name: Domperidone API PowderSynonyms / Chemical Name: Domperidone, 5-Chloro-1-[1-(3-(2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)propyl)-4-piperidinyl]-1,3-dihydro-2H-benzimidazol-2-oneCAS No.: 57808-66-9 Molecular Formula: C₂₂H₂₄ClN₅O₂ Molecular Weight: 425.91 g/mol Appearance: White to off-white crystalline powder Grade: Pharmaceutical/API Grade (IP / BP / USP / EP compliant).

Product Description:
Domperidone API Powder is a high-purity active pharmaceutical ingredient supplied as a white to off-white crystalline powder with an assay typically ≥ 99%. It conforms to major pharmacopeial standards such as IP, BP, USP and EP, ensuring consistent quality and reliability for pharmaceutical manufacturing. Domperidone belongs to the class of dopamine D₂ receptor antagonists and is widely used as a core API in the production of anti-emetic and prokinetic medications — medicines designed to prevent nausea and vomiting and support gastrointestinal motility.
Key Features:High-Purity API Powder: Typically ≥ 99 % assay, suitable for pharmaceutical formulation. White / Off-White Crystalline Powder: Easy to handle, blend and process. Pharmacopeial Compliance: Meets IP, BP, USP, EP quality standards. Consistent Physical Form: Uniform powder for reliable performance in formulation lines. API for Gastrointestinal Agents: Core raw material for anti-emetic, prokinetic and digestive drugs.
Physical & Chemical Properties:Appearance: White to off-white crystalline powder Assay: Typically 99 % minimum (pharmaceutical API) Melting Point: ~241–248 °C (decomposes) Solubility: Slightly soluble in methanol and DMSO; practically insoluble in water. Stability: Stable under recommended storage conditions.
Applications:Pharmaceutical Manufacturing: API for anti-emetic and prokinetic drugs. Gastrointestinal Therapeutics: Used in tablets, capsules, powders and suspensions. Bulk API Supply: Suitable for contract manufacturing, formulation houses and exporters.
Packaging & Storage:Supplied in 25 kg moisture-proof HDPE/fibre drums with internal liners or customized packaging as per buyer requirements. Storage: Keep in a cool, dry, well-ventilated place, protected from moisture, heat and direct sunlight.

Domperidone API
Product Name: Domperidone APISynonyms / Chemical Name: 5‑Chloro‑1‑[1‑(3‑(2‑oxo‑2,3‑dihydro‑1H‑benzimidazol‑1‑yl)propyl)‑4‑piperidinyl]‑1,3‑dihydro‑2H‑benzimidazol‑2‑one; Domperidon; Dopamine Antagonist APICAS No.: 57808‑66‑9 Molecular Formula: C₂₂H₂₄ClN₅O₂ Molecular Weight: ~425.9 g/mol. Appearance: White to off‑white crystalline powder. Grade: Pharmaceutical/API Grade (IP/BP/USP/Ph.Eur). 

Product Description:
Domperidone API is a high‑purity active pharmaceutical ingredient used as the primary bioactive substance in antiemetic and gastroprokinetic drug formulations. Supplied as a white to off‑white fine powder, it is manufactured to conform to international pharmacopoeial standards such as IP (Indian Pharmacopeia), BP (British Pharmacopeia), USP (United States Pharmacopeia) and Ph.Eur (European Pharmacopeia) ensuring consistent quality and reliability for pharmaceutical manufacturers. Domperidone acts as a selective peripheral dopamine D₂/D₃ receptor antagonist, which helps to inhibit nausea and vomiting and also promotes gastrointestinal motility by increasing the contraction frequency in the stomach and intestines. It is widely used in therapeutic formulations to manage symptoms related to delayed gastric emptying, dyspepsia and emesis. 
Key Features:API‑grade powder: High purity and consistency for pharmaceutical applications. White to off‑white crystalline powder with stable physical form. Peripherally acting dopamine antagonist with antiemetic and gastroprokinetic action. Conforms to IP/BP/USP/Ph.Eur specifications. Supplied with COA, MSDS and batch documentation.
Typical Applications:Anti‑Emetic Formulations: Used in tablets, capsules, sachets and oral suspensions to relieve nausea and vomiting. Gastroprokinetic Products: Ingredient in medications that improve gastric emptying and relieve bloating and indigestion. Pharmaceutical Manufacturing: Used by drug makers as the API for finished dosage forms. Veterinary Formulations: Occasionally used in veterinary medicine for similar indications (subject to regional regulations). 
Physical & Chemical Properties:Appearance: White to off‑white crystalline powder. Solubility: Practically insoluble in water; slightly soluble in methanol and ethanol; soluble in organic solvents like DMSO. Melting Point: ~241‑248 °C (decomposes). Purity: Typically ≥ 98 % (API grade).
Packaging & Storage:Available in 25 kg HDPE drums with double liners or customized packaging as per buyer requirements. Store in a cool, dry and dark place, protected from moisture and direct sunlight to maintain stability and shelf life. 

Tenoxicam API Powder – BP/USP/IP Grade (Active Pharmaceutical Ingredient)
Product Name: Tenoxicam APISynonyms: Tenoxicam; 4-Hydroxy-2-methyl-N-pyridin-2-yl-2H-thieno[2,3-e][1,2]thiazine-3-carboxamide 1,1-dioxide CAS Number: 59804-37-4 Molecular Formula: C₁₃H₁₁N₃O₄S₂ Molecular Weight: 337.37 g/mol Grade: BP / USP / IP compliant API (pharmaceutical grade) Physical Form: White to yellowish crystalline powder. Purity/Assay: Typically ≥98% (HPLC).

Description:
Tenoxicam API Powder is a high-quality non-steroidal anti-inflammatory drug (NSAID) active pharmaceutical ingredient used widely in the manufacture of anti-inflammatory and analgesic pharmaceutical products. It belongs to the oxicam class of NSAIDs and is known for its potent anti-inflammatory, analgesic (pain-relieving), and antipyretic (fever-reducing) properties. Tenoxicam works by inhibiting cyclooxygenase (COX-1 and COX-2) enzymes, which play a key role in the synthesis of prostaglandins — biochemical mediators responsible for inflammation, pain, and swelling. This mechanism helps reduce pain and inflammation in conditions such as osteoarthritis, rheumatoid arthritis, musculoskeletal disorders, and acute painful conditions. 
Key Features:Pharmaceutical Grade API: Complies with major pharmacopeial standards (BP/USP/IP) for pharmaceutical manufacturing applications. High Purity & Assay: Typically ≥98% purity ensuring reliable formulation performance. Strong Therapeutic Utility: Core API in NSAID drug products for pain and inflammation relief. Stable Powder Form: Fine crystalline powder suitable for efficient blending and formulation into solid dosage forms like tablets and capsules. Long Half-Life: Enables once-a-day dosing in finished products, enhancing patient compliance (when formulated appropriately).
Applications:Pharmaceutical Manufacturing: Active raw material in the production of anti-inflammatory and analgesic medicines for conditions such as arthritis, musculoskeletal pain, and related disorders. Formulations: Suitable for tablets, capsules or micronized formulations to improve dissolution and bioavailability.Research & Development: Used in formulation development, quality control testing, and analytical method validation.Generic & Branded Products: Ideal for both generic and branded pharmaceutical production worldwide.
Physical & Chemical Properties:Appearance: White to yellowish crystalline powder. Solubility: Very slightly soluble in water; soluble in organic solvents such as methanol or DMSO. Melting Point: Approximately 209–214 °C (decomposition). pH: Near neutral in suspension. (Typical for crystalline APIs).
Storage & Handling:Store in a cool, dry place away from moisture, light, and heat. Keep tightly closed in original containers to preserve quality and prevent degradation.

Cefixime API Powder – Product Description
Product Name: Cefixime API PowderGrade: Pharma Grade / BP / USP / EP (as required).CAS Number: 79350-37-1. Molecular Formula: C₁₆H₁₅N₅O₇S₂. Molecular Weight: ~453.45 g/mol.Appearance: White to off-white crystalline powder.

Description:

Cefixime API Powder is a high-quality active pharmaceutical ingredient (API) used in the manufacture of antibiotic formulations. It belongs to the third-generation cephalosporin class of antibiotics, which are broad-spectrum agents effective against a variety of gram-positive and gram-negative bacterial pathogens. Cefixime works by inhibiting bacterial cell wall synthesis, leading to loss of structural integrity and eventual bacterial cell death, making it a key ingredient for oral antibiotic tablets, capsules, and suspension formulations.
Key Features & Benefits:Pharmacopeial Compliance: Meets BP/USP/EP quality standards (as specified).High Purity: Typically ≥98-99% assay for consistent formulation performance Broad Spectrum: Effective against a wide range of bacterial infections. Excellent Stability: Stable powder form suitable for various pharmaceutical processes.Reliable Source: Manufactured under stringent quality and cGMP environments.
Technical Specifications:Assay (Purity): ≥98-99% (Pharma Grade) Physical Form: Crystalline powder.Solubility: Soluble/almost soluble in appropriate solvents.Melting Point: ~218-225 °C.Packaging: HDPE bags, drums, or as per customer requirement.
Storage & Handling:Store in a cool, dry, and ventilated place.Protect from moisture and light.Use suitable tight containers for long-term storage.

Cefixime API Powder

Product Name: Cefixime API Powder (Active Pharmaceutical Ingredient)CAS No.: 79350-37-1.Molecular Formula: C₁₆H₁₅N₅O₇S₂.Molecular Weight: ~453.45 g/mol.Appearance: White to off-white crystalline powder.Grade: Pharmaceutical Grade API (USP/IP/EP/BP available on request).Packaging: 5 kg / 10 kg / 25 kg HDPE drums / Customized export packaging.

Product Description:
Cefixime API Powder is a high-quality active pharmaceutical ingredient belonging to the third-generation cephalosporin class of antibiotics. It is widely used in the pharmaceutical industry for the manufacture of oral antibiotic formulations such as tablets, capsules, and dry suspensions to treat a broad spectrum of bacterial infections. Cefixime acts by inhibiting bacterial cell wall synthesis, leading to effective bactericidal activity against many Gram-positive and Gram-negative pathogens. This API is supplied as a stable, high-purity crystalline powder, ensuring reliable performance in pharmaceutical formulations and consistent quality for drug manufacturers.
Key Features & Benefits:Pharmaceutical-Grade Quality: Manufactured to meet stringent quality standards with consistent purity and physicochemical properties. Broad-Spectrum Antibiotic API: Effective against a wide range of bacterial infections including respiratory, urinary, and ear-throat infections. Excellent Stability: Good chemical stability and suitable for use in various oral dosage forms. Reliable Supply: Available in bulk quantities with GMP-certified manufacturing and full documentation support (CoA, MSDS). 
Applications:Cefixime API Powder is primarily used in:Pharmaceutical Formulations: For producing tablets, capsules, powders for suspension, and other oral dosage forms. Antibacterial Products: Key ingredient in medicines for treating respiratory tract infections, urinary tract infections, otitis media, throat infections, and other bacterial diseases. Generic API Supply: Supplied to pharmaceutical companies globally for formulation and finishing operations. 
Storage & Handling:Store Cefixime API powder in a cool, dry, and well-ventilated place, away from moisture and direct sunlight. Keep containers tightly closed to preserve quality. Use appropriate PPE (gloves, goggles, masks) while handling to minimize dust exposure.

Cefpodoxime Proxetil Powder API – Product Description

Product Name: Cefpodoxime Proxetil Powder (API)

CAS No.: 117357-91-6

Chemical Name: (±)-Cefpodoxime proxetil

Molecular Formula: C₂₇H₃₀N₄O₈S

Purity: ≥99% (or as per customer requirement)

Appearance: White to Off-White Fine Powder

Category: Pharmaceutical Active Pharmaceutical Ingredient (API)

Product Overview:

 

Cefpodoxime Proxetil is a broad-spectrum third-generation oral cephalosporin antibiotic API used to manufacture pharmaceutical dosage forms. It is widely utilized for its efficacy against a variety of bacterial infections by inhibiting bacterial cell wall synthesis. The API is suitable for formulation into tablets, capsules, and pediatric suspensions.

Key Features & Benefits:

High Purity: Superior grade API with consistent quality and performance.

Pharmaceutical-Grade: Meets strict quality standards for drug manufacturing.

Excellent Stability: Demonstrates chemical stability under recommended storage conditions.

Reliable Supply: Bulk availability with consistent batch-to-batch quality.

 

Formulation-Friendly: Ideal for various oral dosage form developments.

Packaging Options:

1 kg, 5 kg, 10 kg HDPE Bags with Inner PE Liner.

 

Custom packaging per customer requirement.

Storage & Handling:

Store in a cool, dry, and well-ventilated place.

Keep containers tightly closed.

Protect from moisture and direct sunlight.

Follow standard pharmaceutical handling guidelines.

Why Choose Us:

Trusted supplier with global exports.

Competitive pricing and flexible MOQ.

Prompt delivery and responsive customer service.

 

Technical support and tailored solutions available.

Lidocaine HCl IP
Product Name: Lidocaine HCl IP – Pharmaceutical APICAS No.: 73-78-9Chemical Name: Lidocaine Hydrochloride (also known as Lignocaine Hydrochloride).Molecular Formula: C₁₄H₂₂N₂O · HClMolecular Weight: 270.80 g/mol.Grade: Pharmaceutical Grade – IP (Indian Pharmacopoeia).Appearance: White to off-white crystalline powder.Packaging: 1 kg / 5 kg / 25 kg HDPE drums with inner liners (custom export packaging available).

Product Description:
Lidocaine HCl IP is a high-quality active pharmaceutical ingredient (API) widely used in the pharmaceutical industry to manufacture local anesthetic and therapeutic formulations. It is the hydrochloride salt of lidocaine, a well-established amide-type local anesthetic and antiarrhythmic agent. Lidocaine HCl API is supplied as a stable, white crystalline powder with consistent purity and physico-chemical properties, designed for reliable pharmaceutical processing and formulation.
Key Features & Benefits:Pharmaceutical Grade (IP): Manufactured and tested to meet Indian Pharmacopoeia (IP) standards for regulatory compliance and quality. Effective Local Anesthetic: Blocks sodium ion influx in nerve fibers to rapidly produce localized numbness, ideal for dental and minor surgical procedures. Antiarrhythmic Properties: Acts as a Class Ib antiarrhythmic agent, useful in cardiac applications to stabilize ventricular arrhythmias. Versatile Formulation API: Suitable for injectable solutions, topical gels, creams, sprays, and transdermal products. High Purity & Performance: Offers consistent performance in pharmaceutical manufacturing with excellent solubility in water and suitable organic solvents.
Applications:Medical & Dental Anesthesia: Used in the production of injection solutions and topical products for numbing skin, mucous membranes, and deeper tissues during procedures. Pain Management Preparations: Raw material for gels, creams, sprays, and patches designed for localized analgesia. Cardiac Care: Formulated into solutions for intravenous use in managing certain ventricular arrhythmias. Pharmaceutical Manufacturing: Essential API for formulation of finished dosage forms in hospitals, clinics, and commercial drug products.
Storage & Handling:Store Lidocaine HCl IP powder in a cool, dry, and well-ventilated area, away from moisture and direct heat. Keep containers tightly closed to preserve integrity. Handle with appropriate PPE (gloves, mask, goggles) to avoid dust exposure.

Lidocaine Hydrochloride API

Product Name: Lidocaine Hydrochloride API

Synonyms: Lignocaine Hydrochloride, Lidocaine HCl, Xylocaine Hydrochloride, 2‑(Diethylamino)‑N‑(2,6‑dimethylphenyl)acetamide Hydrochloride

CAS No.: 73‑78‑9 

Molecular Formula: C₁₄H₂₂N₂O · HCl 

Molecular Weight: 270.80 g/mol 

Appearance: White to off‑white crystalline powder. 

Grade: Pharmaceutical / API (IP / BP / USP / EP). 

Product Description:

Lidocaine Hydrochloride API is a high‑purity active pharmaceutical ingredient widely used in the global pharmaceutical industry as a local anesthetic and antiarrhythmic agent. It is supplied as a free‑flowing white crystalline powder manufactured to conform with major pharmacopoeial standards such as IP, BP, USP and EP, making it ideal for formulation into a variety of medical products. 

 

Lidocaine Hydrochloride works by blocking sodium ion channels in nerve membranes, inhibiting nerve impulse conduction and producing effective local or regional anesthesia. It has a rapid onset and intermediate duration of action, which makes it a versatile choice for medical, dental and minor surgical procedures. Additionally, its antiarrhythmic properties enable its use in cardiac care.

Key Features:

Pharma‑grade API: Conforms to IP/BP/USP/EP specifications for pharmaceutical use. 

High purity: Typically ≥98 % assay, ensuring consistent performance in formulations. 

White crystalline powder: Easy to handle and process in manufacturing. 

Soluble: Readily soluble in water and alcohol, facilitating formulation into solutions, gels, creams and injectables. 

Rapid action: Fast‑acting anesthetic effect suitable for topical, injectable and procedural applications. 

Versatile applications: Used in both anesthesia and cardiac arrhythmia treatment.

Typical Applications:

Local Anesthetic Formulations: Injectable solutions, dental anesthesia, topical gels and creams for pain relief. 

Antiarrhythmic Products: Component in intravenous formulations for emergency cardiac care. 

Medical & Dental Products: Used in surgical, dermatological and dental procedures to reduce pain. 

Pharmaceutical Manufacturing: Intermediate for advanced formulations and compounded drugs.

Physical & Chemical Properties:

Appearance: White to off‑white crystalline powder. 

Solubility: Soluble in water and alcohol. 

Melting Point: approx. 74‑82 °C.

pH (1 % aq. solution): ~4.0 – 5.5.

Packaging & Storage:

Available in 25 kg HDPE/fiber drums with protective liners or customized pharma packaging. Store in a cool, dry place away from moisture and direct sunlight.

Bronopol BP Powder
Product Name: Bronopol BP Powder.CAS No.: 52-51-7.Molecular Formula: C₃H₆BrNO₄.Molecular Weight: ~199.99 g/mol.

Product Overview:
Bronopol (2-Bromo-2-nitro-1,3-propanediol) is a high-purity white to off-white crystalline powder widely used as an antimicrobial agent, biocide, and preservative across pharmaceutical, cosmetic, and industrial applications. It meets BP (British Pharmacopoeia) quality standards and is supplied in a stable powder form ideal for formulation and manufacturing needs.
Key Specifications:Appearance: White to pale yellow crystalline powder. Purity/Assay: Typically ≥ 98 – 99 % (BP standard).CAS Number: 52-51-7 Form: PowderSolubility: Freely soluble in water and ethanol, slightly soluble in glycerol. pH (1 % w/v): ~5.0 – 7.0. Melting Point: ~123 – 133 °C. Packaging: 25 kg fiber/HDPE drum or as per customer requirement.
Product Features:Pharma/BP Grade Quality: Conforms to BP/Pharmacopoeia standards suitable for regulated formulations. Broad-Spectrum Antimicrobial: Acts effectively against a wide range of bacteria and microorganisms. Stable & Easy-to-Handle Powder: Excellent flow and mixing characteristics.Custom Packaging: Available in industrial packaging for bulk supply.
Applications:Bronopol BP Powder is widely used as a versatile preservative and biocide in:Pharmaceuticals & HealthcarePreservative in liquid medications, syrups, and topical products. Cosmetics & Personal CareUsed in shampoos, lotions, creams, cleansers and toiletries to prevent microbial contamination. Industrial Uses:Water treatment, cooling systems, pulp & paper mills, paints & coatings, adhesives, plastics – controls bacterial growth and prevents biofouling. Household & Consumer Products:Used in formulations such as detergents, cleaning agents, and preservatives to extend product shelf life.
Handling & Safety:Bronopol is an antimicrobial chemical and should be handled using appropriate PPE (gloves, goggles, mask). Store in a cool, dry, well-ventilated area away from heat and incompatible materials. Follow standard industrial safety practices and local regulations during use.
Why Choose Our Bronopol BP Powder:Consistent High Purity: Ensures reliable microbial control in formulations.Wide Applicability: Suitable for pharma, cosmetic, industrial, and household product manufacturing.Documentation & Support: Comes with COA, MSDS, and compliance support for export and regulatory requirements.

Nalidixic Acid API Powder – Product Description
Product Name: Nalidixic Acid API PowderCAS No.: 389-08-2Chemical Name: 1-Ethyl-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylic acidMolecular Formula: C₁₂H₁₂N₂O₃Purity: ≥99% (or as per customer requirement)Appearance: White to Off-White Crystalline PowderCategory: Pharmaceutical Active Pharmaceutical Ingredient (API)

Product Overview:
Nalidixic Acid API is a well-known antibacterial agent belonging to the quinolone class of antibiotics. It is predominantly used in the pharmaceutical industry for the formulation of oral dosage forms indicated for urinary tract infections. With high purity and consistent quality, this API is suitable for bulk drug manufacturing, formulation, and research applications.
Key Features & Benefits:High Purity: Superior quality API with consistent performance.Pharmaceutical-Grade: Conforms to industry standards for drug manufacturing.Stable & Reliable: Good chemical stability under recommended conditions.Formulation Friendly: Easily incorporated into tablets, capsules, and suspension formulations.Excellent Bioavailability: Supports effective therapeutic action in finished dosage forms.
Packaging Options:1 kg / 5 kg / 10 kg / 25 kg HDPE Bags with Inner PE Liner.Customized packaging available as per requirement.
Storage & Handling:Store in a cool, dry, and well-ventilated area.Keep container tightly closed.Protect from moisture and direct sunlight.Handle as per standard pharmaceutical safety guidelines.
Why Choose Us:Trusted supplier with global export experience.Competitive pricing and flexible minimum order quantities (MOQ).Prompt delivery and customer-focused support.Technical assistance and tailored solutions available.

Bronopol API Powder
Product Name: Bronopol API PowderCAS No.: 52-51-7.Chemical Name: 2-Bromo-2-nitro-1,3-propanediol.Molecular Formula: C₃H₆BrNO₄.Molecular Weight: ≈ 199.99 g/mol.Appearance: White to off-white crystalline powder.Grade: API / Industrial / Technical GradePackaging: Custom export packaging (25 kg HDPE drums / bags).

Product Description:
Bronopol API Powder is a high-purity antimicrobial compound widely used in industrial and formulation applications as a broad-spectrum biocide, preservative, and microbiocide. It appears as a white to off-white crystalline powder that is easy to disperse and dissolve in water, providing robust antimicrobial activity. Bronopol is an organic antimicrobial agent known for its effectiveness in controlling microbial growth in a variety of environments—industrial systems, formulations, and water treatment scenarios. It is valued for its stability and reliable performance in preventing bacterial and fungal contamination. 
Key Features & Benefits:High-Purity Powder: Typically supplied with ≥ 98 % purity for consistent performance. Broad-Spectrum Antimicrobial: Effective against a wide range of bacteria and fungi, making it useful for preservative and biocide applications. Water-Soluble & Reactive: Easily dissolves in water for efficient dosing in systems and formulations. Multi-Industry Use: Suitable for industrial water systems, coatings, cosmetics, and preservation formulations. Stable & Reliable: Long shelf life when stored under recommended conditions.
Applications:Bronopol API Powder is widely used in:Industrial Water Treatment: Controls microbial growth in cooling towers, circulating water systems, and paper mills to prevent slime and corrosion. Paints, Coatings & Adhesives: Acts as an in-can preservative to maintain product quality and prevent contamination. Cosmetics & Personal Care: Used as a preservative in shampoos, lotions, creams, and similar products to inhibit bacterial and fungal growth (where permitted). Formulation Preservatives: Suitable for antimicrobial protection in formulations requiring microbiological stability. Pharmaceutical & Healthcare Uses: May be included where biocidal protection is required under regulatory guidelines. 
Storage & Handling:Store Bronopol API Powder in a cool, dry, and well-ventilated place, protected from moisture and direct sunlight. Keep containers tightly sealed to maintain quality and prevent contamination. Use appropriate PPE (gloves, mask, goggles) when handling the powder to avoid inhalation or skin contact.

Meloxicam API Powder
Product Name: Meloxicam API PowderCAS No.: 71125-38-7.Synonyms: Meloxicam, 4-hydroxy-2-methyl-N-(5-methyl-1,3-thiazol-2-yl)-1,1-dioxo-1λ⁶,2-benzothiazine-3-carboxamide.Grade: IP / BP / USP / EP. (Pharmaceutical-Grade Active. Pharmaceutical Ingredient).

Product Overview:
Meloxicam API Powder is a high-quality active pharmaceutical ingredient widely used in the manufacture of anti-inflammatory and analgesic formulations. It belongs to the class of nonsteroidal anti-inflammatory drugs (NSAIDs), recognized for its effectiveness in relieving pain, inflammation, and stiffness associated with arthritis and musculoskeletal conditions.
Chemical & Physical Properties:Chemical Name: MeloxicamMolecular Formula: C₁₄H₁₃N₃O₄S₂.Molecular Weight: ≈ 351.40 g/mol. Appearance: White to light yellow. crystalline powder. Purity: Typically ≥ 99 % (HPLC/assay) per pharmacopeial standards. Solubility: Practically insoluble in water, slightly soluble in strong acids/bases and certain organic solvents. Melting Point: ~254–255 °C. (decomposition). 
Usage & Handling:For pharmaceutical manufacturing and Handle with appropriate PPE (gloves, mask, goggles) in a well-ventilated area.Store in a cool, dry, and ventilated place, protected from moisture and direct sunlight.Refer to supplier-provided MSDS/COA for detailed safety and compliance guidelines.
Packaging & Supply Options:Typically supplied in HDPE drums, fiber drums, or sealed bags (e.g., 25 kg). MOQ and pricing depend on the order size, grade specification, and delivery terms.Technical documentation (COA, MSDS, DMF availability) provided on request.

Lidocaine Hydrochloride BP
Product Name: Lidocaine Hydrochloride BP Synonyms: Lignocaine Hydrochloride BP, Xylocaine Hydrochloride BP, 2‑(Diethylamino)‑N‑(2,6‑dimethylphenyl)acetamide Hydrochloride CAS No.: 73‑78‑9 Molecular Formula: C₁₄H₂₂N₂O·HCl Molecular Weight: ~270.8 g/mol Appearance: White to off‑white crystalline powder. Grade: Pharmacopoeial / BP (British Pharmacopoeia) API.

Product Description:
Lidocaine Hydrochloride BP is a high‑purity pharmaceutical active ingredient manufactured to meet British Pharmacopoeia (BP) standards for use in medical and pharmaceutical formulations. It is supplied as a white to off‑white crystalline powder that is very soluble in water and freely soluble in ethanol, making it suitable for a wide range of dosage forms including injections, topical gels and creams. This compound is the hydrochloride salt form of lidocaine, which functions as a rapid‑onset local anesthetic by blocking sodium channels in nerve cells to inhibit pain signal transmission. It is also classified as a Class IB antiarrhythmic agent and can be used in cardiac care applications under appropriate clinical supervision.
Key Features:BP Pharmacopoeial Quality: Conforms to British Pharmacopoeia specifications for purity and identity. High Purity API: Typical assay range ~99 % on anhydrous basis. White / Off‑white Crystalline Powder: Easy to handle and process in pharmaceutical manufacturing. Solubility: Very soluble in water; freely soluble in ethanol — ideal for various formulations. Rapid Onset of Action: Effective for local anesthesia and pain relief in medical and dental uses. Versatile Use: Suitable for injectable solutions, topical compositions (gels, sprays), and compounded products.
Typical Pharmaceutical Applications:Local Anesthetics: Injectables, nerve blocks, epidural, dental anesthesia. Topical Products: Gels, creams, ointments for pain relief and minor surgical procedures. Antiarrhythmic Agents: Used in hospital settings to manage certain ventricular arrhythmias (when formulated appropriately). Pharmaceutical Manufacturing: Raw material for finished dosage forms requiring anesthetic activity. 
Typical Physical & Chemical Properties:Appearance: White to off‑white crystalline powder Solubility: Very soluble in water; freely soluble in ethanol pH (aqueous solution): Slightly acidic (~4.0–5.5) Assay: NLT 99.0 % and NMT 101.0 % (anhydrous basis) Impurities & Quality: Strict limits on unspecified impurities and sulfated ash to meet BP quality criteria.
Packaging & Storage:Available in 25 kg or 50 kg HDPE/ fiber drums with protective liners or custom pharma‑grade packaging per buyer requirements. Store in a cool, dry place away from moisture and direct sunlight to maintain stability and prevent degradation.

Dobutamine Hydrochloride API 
Product Name: Dobutamine Hydrochloride (Dobutamine HCl) API Powder.CAS No.: 49745-95-1Synonyms: Dobutamine HCl, Dobutrex, Inotrex, Dobutamine hydrochloride, Dl-Dobutamine hydrochloride, β₁-adrenergic agonist API.Molecular Formula: C₁₈H₂₃NO₃·HCl.Molecular Weight: ~337.85 g/mol.

Product Overview:
Dobutamine HCl API Powder is a pharmaceutical-grade active ingredient used as a cardiotonic agent in the production of injectable formulations and finished drug products for cardiovascular support. Supplied as a white to off-white crystalline powder, this API meets pharmacopeial standards (such as USP and EP) and is manufactured under strict quality control for use in pharmaceutical manufacturing and formulation processes.
Key Specifications:Appearance: White to off-white crystalline powder.Assay (Purity): Typically high-purity pharmaceutical grade (e.g., ≥ 98 %).CAS Number: 49745-95-1.Grade: IP / BP / USP / EP as required.Form: Powder (API).Packaging: Export-worthy packaging in drums or customized as per requirement.Storage: Store in a cool, dry, well-ventilated place, protected from light and moisture.
Product Features:Pharmaceutical-Grade API: Conforms to international standards for pharmaceutical usage.Consistent Quality: Ensures reliable performance in drug formulations and manufacturing.Supports Injectable Formulations: Ideal for sterile and injectable cardiotonic products.Documentation Support: Supplied with Certificate of Analysis (COA), MSDS, and related technical documentation.
Applications:Dobutamine HCl API is widely used in the pharmaceutical industry for:Cardiotonic/ Inotropic Drug Formulations: Core API in products designed to increase myocardial contractility and support cardiac output in acute heart failure and cardiac decompensation. Dobutamine works by stimulating β₁-adrenergic receptors in the heart, leading to improved heart pumping function.Injectable Cardiovascular Products: Used to manufacture sterile solutions for intravenous use in clinical settings.Pharmaceutical Manufacturing & R&D: Suitable for bulk manufacturers, contract formulators, and researchers developing cardiovascular drugs.
Handling & Storage:Store Dobutamine HCl API in airtight containers in a cool, dry environment away from heat, light, and moisture. Follow standard pharmaceutical safety practices when handling the API powder. Proper documentation and quality control records should accompany all batches.
Why Choose Our Dobutamine HCl API:High-purity and Pharmaceutical Grade: Suitable for regulated drug production.Regulatory Compliance: Meets global pharmacopeial requirements with documentation.Reliable Supply: Flexible packaging and bulk quantities available for domestic and export markets.Technical Support: Detailed COA, MSDS, and formulation guidance available.

Clotrimazole API Powder – Active Pharmaceutical Ingredient
Product Name: Clotrimazole API PowderCAS Number: 23593-75-1 IUPAC Name: 1-[(2-Chlorophenyl)(diphenyl)methyl]-1H-imidazole Molecular Formula: C₂₂H₁₇ClN₂ Molecular Weight: 344.84 g/mol Appearance: White to off-white crystalline powder Grade: IP / BP / USP / Pharmaceutical Grade Purity: Typically ≥ 98 % (assay on dried basis).

Description:
Clotrimazole is a broad-spectrum antifungal API widely used in the pharmaceutical industry for the manufacturing of topical, oral, and vaginal antifungal medications. It belongs to the imidazole class of antifungals and is effective against a variety of pathogenic fungi by inhibiting ergosterol synthesis in the fungal cell membrane, disrupting membrane integrity and leading to fungal cell death.Key Features & Properties:CAS No: 23593-75-1 Chemical Name: 1-[(2-Chlorophenyl)diphenylmethyl]-1H-imidazole Appearance: White to pale yellow crystalline powder Purity: ≥ 98 % (Pharmaceutical grade) Melting Point: ~147 – 149 °C Solubility: Practically insoluble in water; soluble in organic solvents such as ethanol, methanol, chloroform, and DMSO Storage: Store in a cool, dry place away from light and moisture.
Applications:Clotrimazole API Powder is primarily used as the active ingredient in the formulation of antifungal medications including:Topical creams, ointments, gels, and lotions for skin fungal infections such as athlete’s foot, ringworm, jock itch, and pityriasis versicolor. Vaginal and oral antifungal formulations for yeast infections and candidiasis. Pharmaceutical intermediates and research formulations in antifungal drug development.
Typical Packaging:25 kg / 50 kg HDPE drums with double liners.Export worthy / custom packaging as per buyer requirements.

Tenoxicam API Powder
Product Name: Tenoxicam API PowderSynonyms: 4‑Hydroxy‑2‑methyl‑N‑(pyridin‑2‑yl)‑2H‑thieno[2,3‑e][1,2]thiazine‑3‑carboxamide 1,1‑dioxideCAS No.: 59804‑37‑4.Grade: Pharmaceutical‑Grade API (IP / BP / USP / EP compliant).

Product Overview:
Tenoxicam API Powder is a high‑quality active pharmaceutical ingredient (API) belonging to the non‑steroidal anti‑inflammatory drug (NSAID) class. It is widely used as a raw material in the formulation of anti‑inflammatory, analgesic, and antipyretic pharmaceuticals. Its therapeutic effects include relief from pain, inflammation, and stiffness associated with conditions such as osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, acute musculoskeletal pain, and other inflammatory disorders.
Chemical & Physical Properties:Chemical Name: 4‑Hydroxy‑2‑methyl‑N‑(pyridin‑2‑yl)‑2H‑thieno[2,3‑e][1,2]thiazine‑3‑carboxamide 1,1‑dioxide Molecular Formula: C₁₃H₁₁N₃O₄S₂ Molecular Weight: ≈337.37 g/mol Appearance: White to yellow crystalline powder Purity: Typically ≥98 % (HPLC) pharmaceutical grade. Solubility: Practically insoluble in water; slightly soluble in organic solvents; may be micronized for improved dissolution during formulation. Melting Point: ~209–213 °C (decomposition). Storage: Cool, dry place; protect from light and moisture. 
Key Features & Benefits:Pharmaceutical‑grade API suitable for finished drug formulations. High purity and consistent quality with documentation such as COA and MSDS available on request. Potent analgesic and anti‑inflammatory activity, ideal for NSAID formulations. Stable crystalline powder for ease of handling, storage, and processing. Compliant with global pharmacopeial standards (IP/BP/USP/EP where applicable).
Usage & Handling:For pharmaceutical manufacturing and research use only — not for direct ingestion in raw form.Handle with appropriate PPE (gloves, mask, goggles).Store in a cool, dry, ventilated area, protected from moisture and direct sunlight.Follow all applicable regulatory, safety, and compliance standards for APIs.

Lidocaine Hydrochloride API

Product Name: Lidocaine Hydrochloride API

Synonyms: Lignocaine Hydrochloride, Lidocaine HCl, Xylocaine Hydrochloride, 2‑(Diethylamino)‑N‑(2,6‑dimethylphenyl)acetamide Hydrochloride

CAS No.: 73‑78‑9 

Molecular Formula: C₁₄H₂₂N₂O · HCl 

Molecular Weight: 270.80 g/mol 

Appearance: White to off‑white crystalline powder. 

Grade: Pharmaceutical / API (IP / BP / USP / EP). 

Product Description:

Lidocaine Hydrochloride API is a high‑purity active pharmaceutical ingredient widely used in the global pharmaceutical industry as a local anesthetic and antiarrhythmic agent. It is supplied as a free‑flowing white crystalline powder manufactured to conform with major pharmacopoeial standards such as IP, BP, USP and EP, making it ideal for formulation into a variety of medical products. 

 

Lidocaine Hydrochloride works by blocking sodium ion channels in nerve membranes, inhibiting nerve impulse conduction and producing effective local or regional anesthesia. It has a rapid onset and intermediate duration of action, which makes it a versatile choice for medical, dental and minor surgical procedures. Additionally, its antiarrhythmic properties enable its use in cardiac care.

Key Features:

Pharma‑grade API: Conforms to IP/BP/USP/EP specifications for pharmaceutical use. 

High purity: Typically ≥98 % assay, ensuring consistent performance in formulations. 

White crystalline powder: Easy to handle and process in manufacturing. 

Soluble: Readily soluble in water and alcohol, facilitating formulation into solutions, gels, creams and injectables. 

Rapid action: Fast‑acting anesthetic effect suitable for topical, injectable and procedural applications. 

 

Versatile applications: Used in both anesthesia and cardiac arrhythmia treatment.

Typical Applications:

Local Anesthetic Formulations: Injectable solutions, dental anesthesia, topical gels and creams for pain relief. 

Antiarrhythmic Products: Component in intravenous formulations for emergency cardiac care. 

Medical & Dental Products: Used in surgical, dermatological and dental procedures to reduce pain. 

 

Pharmaceutical Manufacturing: Intermediate for advanced formulations and compounded drugs.

Physical & Chemical Properties:

Appearance: White to off‑white crystalline powder. 

Solubility: Soluble in water and alcohol. 

Melting Point: approx. 74‑82 °C.

 

pH (1 % aq. solution): ~4.0 – 5.5.

Packaging & Storage:

 

Available in 25 kg HDPE/fiber drums with protective liners or customized pharma packaging. Store in a cool, dry place away from moisture and direct sunlight.

Bronopol USP Powder – Pharmaceutical & Industrial Grade
Product Name: Bronopol USP PowderSynonyms: 2‑Bromo‑2‑nitropropane‑1,3‑diol, Bronopol USP, BNPDCAS Number: 52‑51‑7 Molecular Formula: C₃H₆BrNO₄ Molecular Weight: ~199.99 g/mol Grade: USP / BP / IP compliant (pharmaceutical grade preservative) Physical Form: White to off‑white crystalline powder Assay (Purity): ≥99% (typically). 

Product Description:
Bronopol is a high‑performance antimicrobial compound supplied as a white crystalline powder. It is widely used as an effective broad‑spectrum preservative and bactericide, with strong activity against bacteria, fungi, and algae. Its chemical name is 2‑bromo‑2‑nitropropane‑1,3‑diol and it is stable under recommended conditions for use in many formulations.
Key Features:High‑Purity USP Powder: Meets USP/BP/IP standards for pharmaceutical and preservative applications. Broad‑Spectrum Antimicrobial: Effective in controlling microbial contamination in formulations. White Crystalline Powder: Easy to handle and incorporate into solid or liquid formulations. Stable & Water Soluble: Soluble in water and compatible with polar solvent systems.
Applications:Pharmaceutical Preservative: Used in topical pharmaceutical products to prevent microbial growth and increase shelf life. Cosmetics & Personal Care: Employed as a preservative in creams, shampoos, lotions, and other personal care formulations at low concentrations. Industrial Uses: Functions as a microbiocide in water treatment, cooling towers, oil and gas systems, paper mills, and other industrial applications. Surface Sanitizers & Cleaners: Added to disinfectant and surface sanitization products to enhance antimicrobial efficacy.
Typical Specification (Indicative):Assay (HPLC): ≥ 99.0% Appearance: White to off‑white crystalline powder Melting Point: ~130–133 °C Solubility: Soluble in water; sparingly soluble in alcohols and other polar solvents.
Storage & Handling:Store in a cool, dry, and well‑ventilated area away from heat, moisture and direct sunlight. Keep containers tightly closed to maintain product quality. Handle with appropriate personal protective equipment (PPE) such as gloves and eye protection.

Trimethyl Sulfoxonium Iodide (API) Powder – Product Description
Product Name: Trimethyl Sulfoxonium IodideSynonyms: TMSI, Trimethylsulfoxonium iodide, (CH₃O)₃S⁺I⁻CAS Number: 3338-39-6Molecular Formula: (CH₃O)₃S.IMolecular Weight: 211.2 g/mol

Description:
Trimethyl Sulfoxonium Iodide is a high-purity, white to off-white crystalline powder that serves as a potent intermediate in organic synthesis. It is commonly used in pharmaceutical and chemical industries for its ability to introduce sulfonium groups into organic molecules. This compound is widely employed in the production of various complex molecules, such as in the synthesis of chiral compounds and as a reagent in organic reactions like nucleophilic substitution.
Key Features & Benefits:High Purity API Grade: Manufactured under strict quality control to meet industry standards for pharmaceutical use.Versatile Reagent: Highly effective in organic synthesis, particularly in the formation of sulfonium salts and in nucleophilic substitution reactions.Stable & Efficient: Provides excellent stability and ease of handling in various chemical processes.Widely Used in Pharmaceuticals: Ideal for the synthesis of specialty chemicals, chiral intermediates, and active pharmaceutical ingredients (APIs).Chemical Compatibility: Works well in combination with other reagents in organic chemistry, making it a versatile choice for lab and industrial-scale reactions.
Typical Specifications (Indicative):Appearance: White to off-white crystalline powder.Purity: ≥98% (meets API specifications)Molecular Weight: 211.2 g/molMelting Point: ~140°C (range).Solubility: Soluble in water and organic solvents like acetone, methanol, and ethanol.Identification: Matches the IR spectrum of Trimethyl Sulfoxonium Iodide.
Packaging Options:25 g / 50 g / 100 g bottles.1 kg / 5 kg drums (Custom packaging options available).Bulk supply for contract manufacturing and API production.
Storage and Handling:Store in a cool, dry place in a tightly sealed container. Avoid exposure to moisture or air. Handle with appropriate protective equipment such as gloves, goggles, and lab coat to ensure safety during handling.
Why Choose Our Trimethyl Sulfoxonium Iodide Powder?We supply high-quality Trimethyl Sulfoxonium Iodide with consistent purity and reliable performance, suitable for both small-scale research and industrial applications. Our product ensures enhanced synthesis efficiency and superior chemical reactivity, backed by our commitment to timely delivery, competitive pricing, and customized packaging solutions.

Cetirizine Dihydrochloride API Powder – Active Pharmaceutical Ingredient

Product Name: 2‑Chloro BHP Cetirizine / Cetirizine Dihydrochloride

CAS Number: 83881-52-1 

Synonyms: Cetirizine HCl; 2-[4-[(4-Chlorophenyl)phenylmethyl]-1-piperazinyl]ethoxy]acetic acid dihydrochloride 

Molecular Formula: C₂₁H₂₅ClN₂O₃·2HCl 

Molecular Weight: ~461.81 g/mol 

Appearance: White to off-white crystalline powder 

Grade: IP / BP / USP / Pharmaceutical Grade 

Purity: Typically ≥ 98 % assay (HPLC / Pharmacopoeial standard).

Description:

 

Cetirizine Dihydrochloride is a second-generation antihistamine API widely used in the pharmaceutical industry for the formulation of anti-allergy medications. As a highly selective H₁ histamine receptor antagonist, it helps manage and relieve symptoms of allergic conditions such as allergic rhinitis (hay fever), urticaria (hives), dermatitis, and other hypersensitivity reactions.

Key Features & Properties:

CAS No: 83881-52-1 

Chemical Name: Cetirizine dihydrochloride, antihistaminic agent 

Appearance: White to off-white crystalline powder 

Purity: ≥ 98 % (pharmaceutical grade, assay by HPLC/titration) 

Solubility: Soluble in water and methanol; practically insoluble in non-polar solvents. 

Melting Point: ~205 – 225 °C range (pharmacopoeial typical) 

Pharmacological Action: Peripherally selective antihistamine with minimal central sedation compared to first-generation antihistamines. 

 

Hygroscopicity: Slightly hygroscopic crystalline form.

Applications:

Cetirizine Dihydrochloride API Powder is mainly used in the manufacture of pharmaceutical formulations, such as:

Oral tablets and capsules.

Syrups and suspensions.

Chewable tablets.

Pediatric formulations.

Antihistamine combinations and multi-ingredient allergy products.

 

It is essential for anti-allergy and antihistamine drug products designed to relieve symptoms of allergic rhinitis, hay fever, urticaria, and other allergic conditions.

Typical Packaging:

25 kg / 50 kg HDPE drums with protective lining.

Fiberboard drums or cartons.

 

Custom export-grade packaging available on request.

Chlorohexidine Gluconate 20% API.

Product Name: Chlorhexidine digluconate solution 20% / Chlorohexidine Gluconate 20% API.CAS No.: 18472‑51‑0Synonyms: Chlorhexidine digluconate 20% solution, CHG 20%, 1,1’‑hexamethylenebis[5‑(4‑chlorophenyl)biguanide] digluconate.Molecular Formula: C₂₂H₃₀Cl₂N₁₀·2C₆H₁₂O₇, (20% w/v).
Form: Clear liquid solution (colourless to pale yellow).Grade: IP / BP / USP / EP (as required).

Product Overview:
Chlorhexidine Gluconate 20% API is a pharmaceutical‑grade antiseptic and disinfectant active ingredient supplied as a high‑purity liquid solution. It is widely used in healthcare and pharmaceutical formulations for its broad‑spectrum antimicrobial properties, effective against a wide range of bacteria, fungi and some viruses. It serves as a key API in the production of antiseptic gels, surgical scrubs, wound care products and oral hygiene solutions.
Key Specifications:Appearance: Almost colourless to pale yellow, clear liquid. Assay / Purity: Typically 19–21 % w/v active chlorhexidine gluconate CAS No.: 18472‑51‑0. Solubility: Miscible with water; soluble in alcohols and other solvents. pH (typical): ~5.5 – 7.0. Packaging: Drums / IBCs / customized packaging available. Documentation: COA and MSDS provided on request.
Product Features:Pharmaceutical‑grade API: Manufactured to comply with major pharmacopeial standards (IP/BP/USP/EP). Broad‑spectrum antimicrobial activity: Effective against gram‑positive and gram‑negative bacteria, fungi and various pathogens. Stable, clear liquid: Consistent quality and easy formulation handling. Complete documentation: Supplied with COA, MSDS and batch traceability for compliance.
Applications:Chlorhexidine Gluconate 20% API is widely used across pharmaceuticals, healthcare and personal care Antiseptic Formulations: Used in surgical scrubs, hand washes and skin cleansers to control infection risk. Wound Care & Surgical Preparations: Key active ingredient in pre‑operative skin preparation and wound disinfectants. Oral Hygiene Products: Utilized in medicated mouthwashes, dental rinses and periodontal care solutions. Topical Antimicrobials: Ingredient in gels, creams and lotions for skin antisepsis. Medical Devices & Cleaners: Used in cleaning solutions for instruments and catheter disinfection. 
Handling & Storage:Store Chlorhexidine Gluconate 20% API in airtight containers in a cool, dry, well‑ventilated area, away from heat and direct sunlight. Follow standard pharmaceutical safety practices and handle with appropriate PPE.
Why Choose Our Chlorhexidine Gluconate 20% API:Reliable Quality: High‑grade antiseptic API with consistent performance. Regulatory Compliance: Meets global quality standards with full documentation. Versatile Use: Suitable for a range of pharmaceutical and healthcare applications. Bulk Supply & Support: Flexible packaging and supply solutions for exporters and manufacturers.

Minoxidil API Powder – BP/USP/IP Grade (Active Pharmaceutical Ingredient)
Product Name: Minoxidil API PowderSynonyms: Minoxidil; 2,4‑Diamino‑6‑piperidinopyrimidine 3‑oxideCAS Number: 38304‑91‑5 Molecular Formula: C₉H₁₅N₅O Molecular Weight: 209.25 g/mol Grade: BP / USP / IP compliant API (pharmaceutical grade) Physical Form: White to off‑white crystalline powder Purity/Assay: Typically ≥97–99% (HPLC, pharmacopeial standard). 

Description:
Minoxidil API Powder is a high‑purity pharmaceutical active ingredient used primarily in the manufacture of hair growth treatments and dermatological products. It is supplied as a fine crystalline powder that conforms to international pharmacopoeial standards (USP/EP/IP), ensuring consistency and regulatory compliance for pharmaceutical formulation. Originally developed as an antihypertensive vasodilator, Minoxidil’s most common contemporary use is as a topical treatment for hair loss (androgenetic alopecia) in both men and women. It works by stimulating hair follicles and increasing blood circulation at the scalp, promoting hair regrowth and extending the growth (anagen) phase of hair follicles.
Key Features:Pharmaceutical‑Grade API: Designed to meet USP, EP, and IP quality standards for purity and consistency. High Purity: Typically ≥97–99% assay by HPLC, with controlled impurity and drying loss levels. White/Off‑White Powder: Easy to handle and integrate into pharmaceutical manufacturing processes. Versatile Use: Suitable for topical formulations like solutions, foams, gels, sprays, and other hair care products. Regulatory Documentation: Often supplied with COA, MSDS, and other compliance documents on request. 
Applications:Hair Regrowth Products: Core API for topical hair growth solutions, foams, and serums used to treat androgenetic alopecia. Pharmaceutical Manufacturing: For formulation and compounding by manufacturers and pharmacies. Dermatological R&D: Used in research and development of advanced hair care and scalp health products. Combination Formulations: Can be combined with other actives (e.g., finasteride, azelaic acid) in customized topical therapies.
Physical & Chemical Properties:Appearance: White to off‑white crystalline powder. Solubility: Slightly soluble in water; soluble in alcohol, propylene glycol, and some organic solvents. Melting Point: Approx. 248–268 °C (depending on grade and polymorph). Heavy Metals & Impurities: Controlled to pharmacopeial limits (e.g., heavy metals ≤10–20 ppm; total impurities ≤1.5%).
Storage & Handling:Store Minoxidil API in a cool, dry place away from moisture, heat, and direct sunlight. Keep containers tightly sealed to maintain quality, and handle with appropriate protective equipment in a well‑ventilated area.

Hyoscine Butyl Bromide EP 
Product Name: Hyoscine Butyl Bromide EP (Active Pharmaceutical Ingredient)CAS No.: 149-64-4Molecular Formula: C₂₁H₃₀BrNO₄Molecular Weight: ~440.37 g/molSynonyms: N-Butylscopolammonium bromide, Butylscopolamine bromide, Scopolamine N-butyl bromide, Buscopan (API).

Product Overview:
Hyoscine Butyl Bromide EP is a high-quality pharmaceutical-grade active ingredient used in the manufacture of antispasmodic and smooth-muscle relaxant preparations. It is supplied as a white to off-white crystalline powder with consistent purity suitable for formulation into tablets, capsules, and liquid medicines. This EP-grade API meets stringent quality standards required for pharmaceutical production and regulatory compliance.
 OPTION.Storage: Store in a cool, dry place away from moisture and light.Documentation: COA & MSDS available.
Product Features:Pharmaceutical-Grade API: Complies with EP standards for pharmaceutical use.Consistent Quality: High purity and reliable performance in formulations.Wide Compatibility: Suitable for tablets, capsules, syrups, and liquid formulations.Safety Documentation: Supported with COA, MSDS, and regulatory packaging.
Applications:Hyoscine Butyl Bromide EP is widely used in the pharmaceutical industry as a key antimuscarinic API for:Antispasmodic Medicines: Core API for products used in treating smooth muscle spasms of the gastrointestinal (GI) and genitourinary (GU) tracts. Gastrointestinal Formulations: Used in drugs for relief of abdominal cramps, IBS symptoms, and intestinal pain. Urinary Spasm Relief: Effective in formulations addressing bladder and ureteric spasms. Diagnostic & Pre-Procedural Use: Helps reduce smooth-muscle movement in procedures like endoscopy or MRI/CT imaging for clearer results. Pharmaceutical Manufacturing: Suited for bulk manufacturers, contract formulators, and export supply chains.
Handling & Storage:Store Hyoscine Butyl Bromide EP in airtight containers in a cool, dry environment, protected from moisture, heat, and light. Follow industry-standard safety practices when handling the API.
Why Choose Our Hyoscine Butyl Bromide EP:Reliable Quality: Produced under strict quality control for consistent pharmaceutical performance.Regulatory Compliance: Meets EP/USP/IP/BP standards with full documentation support.Flexible Supply: Available in bulk quantities with customizable packaging.Technical Support: Documentation, COA, and compliance assistance included.Our products are supplied to pharmaceutical companies in many international markets including the United States, Canada, Mexico, Brazil, Argentina, Chile, Colombia, Peru, Ecuador, and Uruguay in the Americas.

In Europe, Remedy Labs works with pharmaceutical partners in Germany, France, Italy, Spain, the United Kingdom, the Netherlands, Belgium, Switzerland, Austria, Poland, Portugal, Denmark, Sweden, Norway, Finland, Ireland, Czech Republic, Hungary, Romania, Bulgaria, Greece, and Croatia.Across Asia, our pharmaceutical raw materials are exported to China, Japan, South Korea, Taiwan, Singapore, Malaysia, Thailand, Indonesia, Vietnam, the Philippines, Bangladesh, Sri Lanka, Nepal, Pakistan, Kazakhstan, Uzbekistan, and Mongolia.In the Middle East region, Remedy Labs supplies APIs, pharmaceutical intermediates, and excipients to the United Arab Emirates, Saudi Arabia, Qatar, Oman, Kuwait, Bahrain, Jordan, Lebanon, Iraq, and Iran.Our pharmaceutical ingredients are also distributed across Africa including South Africa, Nigeria, Kenya, Ethiopia, Tanzania, Ghana, Morocco, Algeria, Tunisia, Egypt, Zimbabwe, Zambia, Botswana, and Namibia.In the Oceania region, we serve pharmaceutical companies in Australia, New Zealand, Papua New Guinea, and Fiji.

Cefaclor API Powder – Active Pharmaceutical Ingredient
Product Name: Cefaclor APISynonyms: Cephaclor, Cefaclorum, Ceclor, RaniclorCAS Number: 53994-73-3 Molecular Formula: C₁₅H₁₄ClN₃O₄S Molecular Weight: ~367.8 g/mol Appearance: White to off-white crystalline powder Grade: Pharmaceutical Grade API (BP/USP/EP/IP available on request) Purity: Typically ≥99% (Pharma grade)Packaging: 1 kg / 5 kg / 25 kg bags / drums (custom packaging available).

Product Description:
Cefaclor is a high-quality Active Pharmaceutical Ingredient (API) belonging to the class of second-generation cephalosporin antibiotics. As a broad-spectrum antimicrobial agent, Cefaclor API is used in the manufacture of oral antibiotic formulations for the treatment of a variety of bacterial infections. Chemically, it is defined as a semisynthetic cephalosporin with a cephem core structure and specific functional groups that provide effective activity against many Gram-positive and selected Gram-negative bacteria.
Key Features & Benefits:Pharmaceutical-Grade API – Manufactured to meet global pharmacopeial standards (BP/USP/EP/IP) for quality and safety. High Purity & Consistency – Ensures reliable performance in finished dosage forms such as tablets, capsules, and suspensions. Broad-Spectrum Antibiotic – Used in formulations targeting respiratory, skin, urinary tract and other bacterial infections (finished products). Stable Powder Form – Easy to handle, store, and incorporate into pharmaceutical processes. Custom Packaging Available – Flexible packaging for domestic and export markets.
Applications:API for oral antibiotic formulations (tablets, capsules, dry powders for suspension).Used in pharmaceutical R&D, formulation development, and quality control.Suitable for international exports with compliance to key pharmacopeias.
Storage & Handling:Store in a cool, dry, well-ventilated place. Protect from moisture and direct sunlight. Keep containers tightly closed when not in use to maintain API quality.

Ambroxol HCl USP Powder – Pharmaceutical Grade API
Product Name: Ambroxol Hydrochloride (Ambroxol HCl) USP PowderChemical Name: trans-4-[(2-Amino-3,5-dibromobenzyl)amino]cyclohexanol hydrochlorideCAS Number: 23828-92-4Molecular Formula: C₁₃H₁₈Br₂N₂O·HCl Molecular Weight: ~414.56 g/mol Appearance: White to off-white crystalline powder Grade: USP / IP / BP / EP (pharmacopeial)Purity: ≥ 99.0% (or as per customer requirement)

Description:
Ambroxol HCl USP Powder is a high-quality active pharmaceutical ingredient (API) used predominantly in the formulation of respiratory medicines. It acts as a mucolytic and expectorant agent, helping to thin and loosen mucus in the airways, making it easier to cough up and clear from the respiratory tract. This improves breathing in patients with respiratory conditions associated with excessive or thick mucus.
Key Features & Benefits:Pharmaceutical-grade quality: Conforms to USP standards for API use in drug manufacturing. High purity and consistency: ≥99% purity with strict quality control and Certificate of Analysis (COA) available. White crystalline powder: Easy to handle, process, and formulate. Versatile API: Suitable for a variety of respiratory formulations (tablets, syrups, inhalation solutions). Stable with good shelf life: Long-term stability under recommended storage conditions.
Technical Specifications:Purity (HPLC): ≥ 99.0%Appearance: White to off-white crystalline powder. Solubility: Soluble in organic solvents, sparingly soluble in water. Melting Point: ~235-240°C.Assay & Impurity Limits: Complies with pharmacopeial standards.
Packaging & Storage:Standard Packing: 1 kg, 5 kg, 25 kg drums (custom packing available).Storage: Store in a cool, dry place, protected from moisture and direct sunlight.Shelf Life: Typically 3–5 years under recommended conditions.

Ambroxol HCl BP Powder – Pharmaceutical Grade API
Product Name: Ambroxol Hydrochloride BP PowderChemical Name: trans-4-[(2-Amino-3,5-dibromobenzyl)amino]cyclohexanol hydrochlorideCAS Number: 23828-92-4Molecular Formula: C₁₃H₁₈Br₂N₂O·HClMolecular Weight: ~414.56 g/molAppearance: White to off-white crystalline powder.Grade: BP (British Pharmacopoeia) / IP / USP / EP pharmaceutical standard.Purity: ≥ 99.0% (or as per customer requirement)

Description:

Ambroxol HCl BP Powder is a pharmaceutical-grade active pharmaceutical ingredient (API) commonly used in the manufacture of mucolytic and expectorant formulations. It is an effective agent that helps thin and loosen thick mucus in the respiratory tract, aiding easier expectoration in conditions such as bronchitis, COPD, asthma, and other respiratory disorders.
Key Features & Benefits:BP-grade quality conforming to British Pharmacopoeia with global market acceptance.High purity ≥ 99% ensuring consistent performance in pharmaceutical products.White to off-white crystalline powder — easy to handle and process.Excellent solubility profile in suitable solvents for formulation processes.Stable and long shelf life under recommended storage conditions.Comprehensive documentation — Certificate of Analysis (COA) and MSDS available.
Technical & Physical Specifications:Appearance: White to almost white crystalline powder Solubility: Sparingly soluble in water, soluble in methanol (typical for Ambroxol HCl) Melting Point: Around 235–240°C (varies slightly with grade) Assay (HPLC): ≥ 99% pharmaceutical grade
Packaging & Storage:Standard Packaging: 1 kg, 5 kg, 25 kg drums or customized options.Storage: Store in a cool, dry place away from moisture and direct sunlight.Shelf Life: Typically up to 3–5 years under recommended conditions.

Ambroxol HCl IP Powder – Pharmaceutical Grade API
Product Name: Ambroxol Hydrochloride IP PowderChemical Name: Ambroxol hydrochloride (trans-4-[(2-Amino-3,5-dibromobenzyl)amino]cyclohexanol hydrochloride)CAS Number: 23828-92-4Molecular Formula: C₁₃H₁₈Br₂N₂O·HCl Molecular Weight: ~414.56 g/mol Appearance: White to off-white crystalline powder Grade: IP (Indian Pharmacopoeia) / BP / USP pharmaceutical standard Purity: ≥ 99.0% (or as per customer requirement)

Description:
Ambroxol HCl IP Powder is a high-quality pharmaceutical active ingredient (API) widely used in the formulation of respiratory medicines. It functions as a mucolytic and expectorant agent, helping to break down and thin mucus, promoting easier clearance from the respiratory tract. This makes it highly suitable for treating conditions associated with thick or excessive mucus, including bronchitis, COPD, asthma, and other respiratory disorders.
Key Features & Benefits:Pharmaceutical-grade quality meeting IP standards and suitable for global markets High purity ≥ 99% with consistent batch-to-batch performance White crystalline powder — easy to handle, process and formulate Versatile API suitable for multiple dosage forms including tablets, syrups, and inhalation solutions Comprehensive testing with Certificate of Analysis (COA) and MSDS available on request.Long shelf life under recommended storage conditions.
Physical & Chemical Properties:Appearance: White to off-white crystalline powder. Solubility: Soluble in methanol, sparingly soluble in water.pH: Typically between ~4.5–6.0 (5% solution).Assay (HPLC): ≥ 99% pharmaceutical grade.
Packaging & Storage:Standard Packaging: 1 kg, 5 kg, 25 kg drums or customized as per requirement Storage: Store in a cool, dry place, protected from moisture and direct sunlight Shelf Life: Typically up to 5 years if stored under recommended conditions

Chlorzoxazone Powder API
Product Name: Chlorzoxazone Powder APICAS No.: 95-25-0.Synonyms: 5-Chloro-2-benzoxazolone; Paraflex; Mioran.Grade: IP / BP / USP (Pharmaceutical-Grade).

Product Overview:
Chlorzoxazone Powder API is a high-quality active pharmaceutical ingredient (API) used in the manufacture of muscle relaxant medicines. It is a centrally acting skeletal muscle relaxant that helps relieve pain and stiffness caused by muscle strains and spasms.
Chemical & Physical Properties:Chemical Name: Chlorzoxazone.Molecular Formula: C₇H₄ClNO₂.Molecular Weight: ~169.56–169.57 g/mol. Appearance: White to off-white crystalline powder. Purity: Typically ≥98% (or as specified) depending on supplier. Melting Point: ~191–192 °C. Solubility: Slightly soluble in water; soluble in common organic solvents such as ethanol, acetone, chloroform.
Key Features & Benefits:Pharmaceutical-grade API: Suitable for formulation into solid oral dosage forms such as tablets and capsules. Consistent quality & purity: Manufactured to meet pharmacopeial standards (IP/BP/USP) with documentation like COA/MSDS available on request. Stable powder form: Micronized and easy for handling and processing. Long shelf life: Stable under recommended storage conditions (cool, dry, away from light).
Usage & Handling:Intended strictly for pharmaceutical manufacturing and R&D use (not for direct ingestion in raw form).Store in a cool, dry, well-ventilated place, protected from moisture and direct sunlight.Follow applicable safety and regulatory standards during handling.

Product Description — Clomiphene Citrate API Powder
Clomiphene Citrate API Powder is a high-quality, pharmaceutical-grade active pharmaceutical ingredient (API) supplied as a white to pale yellow crystalline powder. It is widely used in the manufacture of fertility drugs and ovulation stimulants under recognized pharmacopeial standards such as IP / BP / USP for consistent performance and regulatory compliance.
Key Features:Chemical Name: Clomiphene Citrate (Selective Estrogen Receptor Modulator, SERM) CAS Number: 50-41-9 Molecular Formula: C₃₂H₃₆ClNO₈ Appearance: White to pale yellow crystalline powder. Purity (Assay): ≥ 98 % (typical API grade) Solubility: Slightly soluble in water; soluble in organic solvents such as methanol and ethanol Melting Point: Approx. 116–118 °C
Functional Benefits:Clomiphene citrate is a selective estrogen receptor modulator that helps stimulate the release of gonadotropins (LH & FSH) by blocking estrogen’s negative feedback on the hypothalamic-pituitary axis. This mechanism induces ovulation, making it essential in fertility treatment formulations.
Storage & Packaging:Storage: Keep in a cool, dry, and light-protected environment to maintain stability and shelf life. Packaging: Available in customized bulk packaging (e.g., HDPE drums with inner liners, vacuum sealed bags) as per buyer requirements.

Tinidazole API Powder
Product Name: Tinidazole API PowderSynonyms: Nitroimidazole derivative, 1‑(2‑ethylsulfonylethyl)‑2‑methyl‑5‑nitroimidazoleCAS No.: 19387‑91‑8Grade: IP / BP / USP. Pharmaceutical‑Grade Active. Pharmaceutical Ingredient.

Product Overview:
Tinidazole API Powder is a high‑quality active pharmaceutical ingredient (API) used as the key raw material in the manufacture of antiprotozoal and antibacterial medications. It belongs to the nitroimidazole class of compounds and is valued for its broad antimicrobial activity, particularly against anaerobic bacteria and protozoa.
Chemical & Physical Properties:Chemical Name: 1‑(2‑ethylsulfonylethyl)‑2‑methyl‑5‑nitroimidazole. Molecular Formula: C₈H₁₃N₃O₄S. Molecular Weight: ≈ 247.27 g/mol. Appearance: White to off‑white crystalline powder. Purity: Typically ≥ 98–99 % (HPLC/assay) pharmaceutical grade. Solubility: Slightly soluble in water; soluble in organic solvents such as methanol and acetone. Melting Point: Approx. 127–130 °C. 
Key Features & Benefits:Pharmaceutical‑grade API compatible with IP, BP, and USP standards (COA & MSDS available on request). Consistent high purity and quality ideal for formulation and bulk API supply. Broad antimicrobial activity effective for antiprotozoal and antibacterial drug development. Stable crystalline powder for ease of handling, storage, and pharmaceutical processing. Long shelf life when stored under recommended conditions (cool, dry, and away from light).
Usage & Handling:For pharmaceutical manufacturing and R&D use only (not for direct human consumption in raw form).Store in a cool, dry, ventilated area away from moisture, heat, and direct light.Handle using appropriate PPE (gloves, mask, goggles).Follow applicable regulatory, safety, and compliance standards for APIs.