Remedy Labs

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

Guaifenesin API Powder
Product Name: Guaifenesin USP 36 Powder Bulk (Guaifenesin API Powder)CAS No.: 93-14-1.Synonyms: Guaiphenesin, Glyceryl guaiacolate, 3-(2-Methoxyphenoxy)-1,2-propanediol.Grade: IP / BP / USP / Pharma-Grade Active Pharmaceutical Ingredient.

Product Overview:
Guaifenesin API Powder is a high-quality active pharmaceutical ingredient widely used in the pharmaceutical industry for the formulation of expectorant medicines. It is a key raw material in the manufacture of cough and cold therapeutic products and is valued for its ability to help loosen and thin mucus in the airways, making it easier to cough up and clear congestion.
Chemical & Physical Properties:Chemical Name: 3-(2-Methoxyphenoxy)-1,2-propanediol. Molecular Formula: C₁₀H₁₄O₄. Molecular Weight: ≈ 198.22 g/mol. Appearance: White to slightly gray crystalline powder. Melting Point: ~78–82 °C. Solubility: Soluble in water, alcohol and some organic solvents. Assay: Typically ≥ 98–99 %. 
Key Features & Benefits:Pharmaceutical-grade API compliant with global pharmacopeial standards (IP/BP/USP). High chemical purity and consistent quality for reliable formulation results. Supplied in stable crystalline powder form for easy handling and processing. Suitable for incorporation into a wide range of finished dosage forms such as tablets, capsules, syrups, and powders. Long shelf life when stored under recommended conditions (cool, dry, and away from light).
Usage & Handling:For pharmaceutical manufacturing and R&D use only.Store in a clean, cool, dry area in tightly closed containers. Use appropriate personal protective equipment (PPE) during handling.Follow standard regulatory and safety protocols.

Lidocaine Base IP – Active Pharmaceutical Ingredient
Product Name: Lidocaine Base (IP Grade)CAS Number: 137-58-6 Molecular Formula: C₁₄H₂₂N₂O Molecular Weight: 234.34 g/mol Pharmacopoeia Standard: IP (Indian Pharmacopoeia) / BP / USP / EP Grade: IP Pharmaceutical Grade API Appearance: White to off-white crystalline powder. Purity: ≥99% (Typical assay) Packaging: 25 kg HDPE drum / Fiber drum (export standard).

Description:
Lidocaine Base IP is a high-quality Active Pharmaceutical Ingredient (API) used in the formulation of local anesthetics and antiarrhythmic drugs. It is produced to meet the Indian Pharmacopoeia (IP) standards, ensuring compliance with regulatory requirements for pharmaceutical manufacturing in India and for export. Chemically, Lidocaine is an amide-type local anesthetic that works by blocking voltage-gated sodium channels in nerve fibers, thereby inhibiting the initiation and conduction of nerve impulses which results in effective local numbness and anesthesia.
Key Features & Benefits:IP Compliant API — Manufactured in accordance with Indian Pharmacopoeia standards for pharmaceutical use. High Purity & Consistency — Typically ≥99% assay ensures dependable performance in finished formulations. Versatile Application — Used in topical, injectable, and other dosage forms for pain relief and anesthesia. Broad Pharmaceutical Use — Suitable for creams, gels, ointments, sprays, patches, and injectables. Stable & Reliable — Good shelf-life and stability under recommended storage conditions. 
Applications:Local anesthesia in minor surgical procedures, dental applications, and dermatological treatments. Formulation of topical analgesics (creams, ointments, gels) to relieve itching, pain or burning. Intermediate for pharmaceutical synthesis and compounding.
Storage & Handling:Store in a cool, dry, well-ventilated place away from direct heat and moisture. Ensure packaging is sealed when not in use to maintain quality and stability.

Lidocaine Base API — Active Pharmaceutical Ingredient
Product Name: Lidocaine Base APICAS Number: 137-58-6 Molecular Formula: C₁₄H₂₂N₂O Molecular Weight: ~234.34 g/mol IUPAC Name: 2-(diethylamino)-N-(2,6-dimethylphenyl) acetamide Synonyms: Lidocaine, Lignocaine, Xylocaine Appearance: White to off-white crystalline powder. Grade: Pharma / IP / BP / USP / EP (as per customer requirement). Purity: ≥99% (Pharmaceutical grade). Packaging: 25 kg HDPE drum (export. standard) / custom packaging available.

Description:
Lidocaine Base is a widely used local anesthetic API of the amide type, employed in the manufacturing of pharmaceutical formulations for pain management and minor surgical procedures. It acts by blocking voltage-gated sodium channels in nerve cells, interrupting pain signal transmission and providing effective local or regional anesthesia. This API is essential in the production of injectable solutions, topical gels, creams, ointments, sprays, and patches designed to provide rapid onset pain relief.
Key Features & Benefits:High-Purity API — Meets stringent pharmacopoeial standards (IP/BP/USP/EP). Effective Local Anesthetic — Provides rapid and reliable pain control. Versatile Applications — Used in dermatological, dental, surgical, and emergency care formulations. Fast Onset of Action — Quickly numbs targeted areas for efficient procedural use. Stable & Well-Characterized — Good shelf life with consistent performance in finished formulations. Cost-Effective — Ideal for bulk API requirements in pharmaceutical manufacturing.
Typical Applications:Local and regional anesthesia in minor medical and dental procedures. Topical analgesic products (creams, gels, sprays). Used as API in formulations to manage certain cardiac arrhythmias (class-IB antiarrhythmic). Intermediate in pharmaceutical synthesis and compound development. 
Storage & Handling:Store in a cool, dry place away from direct sunlight. Ensure containers are tightly sealed to maintain stability and potency. Handle with appropriate safety measures according to good manufacturing practices.

Tamoxifen Citrate API
Product Name: Tamoxifen Citrate API.CAS No.: 54965-24-1. 

Product Description:
Tamoxifen Citrate is an active pharmaceutical ingredient (API) belonging to the class of selective estrogen receptor modulators (SERMs) with potent antiproliferative and antitumor properties. It is widely used in the manufacture of anti-breast cancer formulations, and is a key raw material for therapeutic applications in oncology. 
Chemical & Physical Properties:Chemical Name: (Z)-2-[4-(1,2-Diphenyl-1-butenyl)phenoxy]-N,N-dimethylethanamine citrate. Molecular Formula: C26H29NO·C6H8O7. Molecular Weight: ~563.64 g/mol. Appearance: White to off-white crystalline powder. Solubility: Soluble in methanol; slightly soluble in ethanol; very slightly soluble in water. Melting Point: ~140–148 °C. 
Key Features:High-purity API for pharmaceutical manufacturing & research use. Manufactured under cGMP/ISO quality standards (depending on supplier). Suitable for oncology drug formulations and intermediates. 
Pharmacological Role:Tamoxifen citrate is a selective estrogen receptor modulator (SERM) that:Blocks estrogen receptors on breast cancer cells.Prevents estrogen-stimulated tumor growth.Is extensively used in hormone-dependent breast cancer treatment and adjuvant therapy.
Usage & Handling:For manufacturing and laboratory use only (not for direct consumption).Store in a cool, dry place at controlled temperature (e.g., 2–8 °C). Follow all regulatory, safety and compliance standards for APIs during handling.
Packaging & Supply:Typically supplied in:Drum, Bag, or HDPE containers.Custom packaging available upon request.Bulk quantities supported for commercial orders.
Applications:Oncology drug formulations.Pharmaceutical intermediate for breast cancer medicines.Research & development API supply.

Letrozole API Powder – Active Pharmaceutical Ingredient
Product Name: Letrozole APICAS Number: 112809-51-5 IUPAC Name: 4-[(4-cyanophenyl)-(1,2,4-triazol-1-yl)methyl]benzonitrile Molecular Formula: C₁₇H₁₁N₅ Molecular Weight: 285.30 g/mol Pharmacopoeia Standards: IP / BP / USP (available on request) Appearance: White to off-white crystalline powder Assay (Purity): Typically ≥99% (HPLC/Pharmacopeial assay) Specification: Complies with IP/BP/USP quality standards Packaging: 1 kg – 25 kg bags / drums (custom packaging available)Storage: Store in a cool, dry place, protected from moisture, heat and direct sunlight.

Description:
Letrozole API Powder is a high-purity active pharmaceutical ingredient manufactured to meet strict IP (Indian Pharmacopoeia), BP (British Pharmacopoeia), and USP (United States Pharmacopeia) standards for pharmaceutical use. It is supplied as a white to off-white crystalline powder with excellent physicochemical properties and consistent batch-to-batch quality. Letrozole is a non-steroidal aromatase inhibitor that works by inhibiting the aromatase enzyme responsible for converting androgens to estrogen in the body. This mechanism of action makes it an essential API for oncology drug formulations, particularly in the treatment of hormone-responsive breast cancer in postmenopausal women.
Key Features & Benefits:Pharmaceutical-Grade API — Manufactured to meet IP/BP/USP pharmacopeial standards. High Purity & Consistent Quality — Typically ≥99% assay ensures reliable performance in finished products. White to Off-White Powder Form — Easy to handle and incorporate into oral dosage forms. Versatile Application — Ideal for tablets, capsules, and other solid oral formulations. Regulatory Compliance — Suitable for global markets requiring pharmacopeial compliance. Secure Packaging — Export quality packaging options for safe storage and transport.
Applications:API for oncology pharmaceutical formulations, especially hormone-responsive breast cancer therapies. Use in R&D and formulation development of aromatase inhibitor drugs. Suitable for domestic and international pharmaceutical manufacturing.
Storage & Handling:Store in a cool, dry, well-ventilated area away from moisture and direct heat. Ensure packaging is sealed and protected from light to maintain stability and preserve API quality.

Isopropyl Chloroacetate (IPCA) API Powder – Product Description
Product Name: Isopropyl Chloroacetate (IPCA) API PowderCAS No.: 1642-95-3Purity: ≥99% (or specify grade)Form: White to Off-White Crystalline PowderGrade: Industrial / Technical / Pharma Intermediate.

Product Overview:
Isopropyl Chloroacetate (IPCA) is a high-purity chemical intermediate widely used in organic synthesis and pharmaceutical manufacturing. Known for its excellent reactivity and stability, IPCA plays a key role in the synthesis of active pharmaceutical ingredients (APIs), agrochemicals, fragrances, and specialty chemicals.
Key Features & Benefits:High Purity: Manufactured under controlled conditions for consistent quality.Stable & Reliable: Minimal impurities ensure dependable performance in chemical reactions.Versatile Intermediate: Suitable for various organic synthesis and formulation applications.Good Solubility: Easily soluble in many organic solvents aiding smooth processing.Quality-Assured: Tested for appearance, purity, and performance parameters.
Packaging Options:1 kg / 5 kg / 25 kg HDPE Drums.Custom Packaging available on request.
Safety & Handling:Store in a cool, dry place, in a tightly closed container. Handle in accordance with recommended safety practices.
Why Choose Us:Trusted Supplier with consistent quality.Competitive pricing and bulk availability.Prompt delivery and responsive customer support.Customization and technical support available. 

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. 

Sildenafil Citrate API (IP Grade) – Product Description

Product Name: Sildenafil Citrate.Grade: IP (Indian Pharmacopoeia) / BP / USP / EP available.CAS Number: 171599-83-0. Molecular Formula: C₂₂H₃₀N₆O₄S · C₆H₈O₇ (citrate salt). Molecular Weight: ~666.7 g/mol. Appearance: White to off-white crystalline powder. 

Description:
Sildenafil Citrate API is a pharmaceutical-grade active ingredient used for the manufacture of oral dosage forms targeting erectile dysfunction and pulmonary arterial hypertension (PAH). It is a selective phosphodiesterase type-5 (PDE5) inhibitor that enhances nitric-oxide-mediated vasodilation and increases blood flow to targeted tissues.
Key Pharmaceutical Features:Mechanism: Selective inhibition of PDE5 enzyme leading to increased cGMP levels and smooth muscle relaxation. Therapeutic Category: PDE5 inhibitor (Erectile dysfunction / PAH). API Applications: Raw material for tablets, capsules, and other finished formulations. Pharmacopoeial Compliance: Meets IP standards (with BP/USP/EP also supported upon request).
Technical Specifications:Purity (Assay): ≥99.0% (typical pharma grade). Solubility: Freely soluble in DMSO/ethanol; slightly soluble in water. Melting Point: ~186–192 °C. Form: Powder, suitable for formulation use.
Packaging & Storage:Standard Packaging: 25 kg HDPE drum with inner poly liners (custom packaging on request). Storage Conditions: Store in a cool, dry place away from moisture, heat, and direct sunlight. Shelf Life: Typically 2–5 years if stored correctly. 
Regulatory & Quality Compliance:Certificate of Analysis (COA) and Material Safety Data Sheet (MSDS) available. Manufactured under cGMP standards; export-ready API suitable for regulated markets.

Sildenafil Citrate API

Product Name: Sildenafil Citrate API – Pharmaceutical Active Ingredient

CAS No.: 171599‑83‑0

Chemical Name: Sildenafil Citrate.

Molecular Formula: C₂₂H₃₀N₆O₄S · C₆H₈O₇

Molecular Weight: ≈ 666.7 g/mol.

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

Appearance: White to off‑white crystalline powder.

Packaging: Standard export packaging (25 kg HDPE drums with inner liners / custom packaging available).

Product Description:

Sildenafil Citrate API is a high‑purity pharmaceutical active ingredient widely used by pharmaceutical manufacturers in the formulation of oral medicines for the treatment of erectile dysfunction (ED) and pulmonary arterial hypertension (PAH). It is a selective phosphodiesterase type‑5 (PDE5) inhibitor that enhances blood flow by preventing the breakdown of cyclic GMP in vascular smooth muscle cells. 

 

Supplied as a stable, white to off‑white crystalline powder, this API meets stringent pharmacopeial standards (IP/USP/BP/EP) and is suitable for use in tablets, capsules, and other solid oral dosage forms. 

Key Features & Benefits:

Pharmaceutical‑Grade API: Manufactured to meet major pharmacopoeial standards (IP/USP/BP/EP) with high purity and consistent quality. 

Selective PDE5 Inhibitor: Acts by inhibiting phosphodiesterase type‑5, helping to improve blood flow in targeted tissues. 

Wide Application: Primarily used in formulations for erectile dysfunction and pulmonary arterial hypertension. 

Reliable Supply: Comes with Certificate of Analysis (CoA) and MSDS documentation. 

 

Consistent Performance: Excellent physico‑chemical properties ensure reliable results in formulation and manufacturing processes.

Applications:

Erectile Dysfunction (ED) Medicines: Core ingredient in oral formulations designed to enhance erectile response. 

Pulmonary Arterial Hypertension (PAH): Used in drug products to help relax pulmonary blood vessels and improve exercise capacity. 

Pharmaceutical Manufacturing: Ideal for tablets, capsules, and other solid dose forms targeting cardiovascular and urological indications. 

 

API R&D & Formulation Development: Used in research and new product development.

Storage & Handling:

 

Store Sildenafil Citrate API in a cool, dry, and well‑ventilated area, protected from moisture and direct sunlight. Keep containers tightly sealed to maintain product integrity. Handle with appropriate PPE (gloves, mask, goggles) to avoid inhalation of fine particles.

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.

Lidocaine Base Powder API
Product Name: Lidocaine Base Powder APICAS No: 137-58-6.Molecular Formula: C₁₄H₂₂N₂O.Molecular Weight: 234.34 g/mol.Appearance: White to off-white crystalline powder.Grade: Pharma Grade (IP/BP/USP/EP)Form: Powder.Packaging: HDPE drum / export standard packaging.

Product Description:

Lidocaine Base Powder API is a high-quality active pharmaceutical ingredient (API) used extensively in the pharmaceutical industry for producing local anaesthetic and therapeutic formulations. It belongs to the amide class of local anaesthetics and is widely recognized for its rapid onset of action and reliable performance in pain management applications. This API is supplied as a white to off-white crystalline powder with excellent purity and consistency, suitable for further processing into injectable formulations, topical gels, creams, ointments, sprays, and other medicated products.
Key Features:Pharmaceutical-Grade Quality: Manufactured to meet stringent global standards — IP, BP, USP, and EP — ensuring high purity and batch-to-batch consistency. Effective Local Anaesthetic: Blocks nerve signal transmission by inhibiting sodium channels, delivering prompt and effective numbness in targeted areas. Versatile API Use: Ideal for formulating a range of products including topical anesthetics, dental anesthetics, and surgical pain-relief preparations. Stable & Easy to Handle: Suitable for storage under standard conditions and compatible with various excipients in pharmaceutical formulations. 
Applications:Lidocaine Base Powder API is widely used in:Local anaesthetic formulations for minor surgical and dental procedures. Topical analgesic products such as gels and creams for skin and mucous membrane pain relief. Injectable anaesthetics for clinical use in hospitals and dental clinics. Pharmaceutical manufacturing as a key raw material in pain-management and anti-arrhythmic preparations.
Storage & Handling:Store in a cool, dry, and well-ventilated place, away from direct sunlight, moisture, and heat. Use proper handling procedures and personal protective equipment to maintain product integrity and safety.

Piroxicam API Powder 
Product Name: Piroxicam API Powder – Pharmaceutical Active IngredientCAS No.: 36322-90-4.Chemical Name: 4-Hydroxy-2-methyl-N-(pyridin-2-yl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide.Molecular Formula: C₁₅H₁₃N₃O₄S.Molecular Weight: 331.35 g/mol.Appearance: Yellow to light yellow crystalline powder.Grade: Pharmaceutical API Grade (BP/USP/IP applicable).Packaging: 5 kg / 10 kg / 25 kg HDPE drums or custom export packaging available.Shelf Life: Up to 5 years (when stored properly).

Product Description:
Piroxicam API Powder is a high-quality active pharmaceutical ingredient (API) used in the manufacture of non-steroidal anti-inflammatory drugs (NSAIDs) for pain relief and management of inflammatory conditions. It is widely used by pharmaceutical companies in the production of tablets, capsules, and other oral dosage forms targeting symptoms such as pain, stiffness, and swelling associated with arthritis, musculoskeletal disorders, and inflammatory diseases.
Key Features & Benefits:Pharmaceutical-Grade Quality: Manufactured to meet global pharmacopeial standards (BP/USP/IP) with consistent quality and purity. Effective NSAID API: Acts as a key ingredient in anti-inflammatory formulations that inhibit prostaglandin synthesis, helping reduce pain, swelling, and stiffness. Good Stability: Stable crystalline powder with long shelf life when stored under recommended conditions. Reliable Performance: Suitable for use in large-scale pharmaceutical manufacturing with uniform physicochemical properties. Document Support: Certificate of Analysis (CoA), MSDS, and other compliance documents available on request. 
Applications:Piroxicam API Powder is widely used in:Pharmaceutical Manufacturing: Core API for NSAIDs used in analgesic and anti-inflammatory drug products. Pain & Inflammation Therapeutics: Formulations to manage osteoarthritis, rheumatoid arthritis, musculoskeletal pain, and related conditions. Clinical R&D: Research and development of generic and specialty anti-inflammatory formulations.
Storage & Handling:Store Piroxicam API Powder in a cool, dry, and well-ventilated area, protected from moisture, direct heat, and light. Keep the container tightly closed when not in use. Use appropriate PPE (gloves, mask, goggles) during handling to avoid inhalation of fine powder and maintain product quality.

Product Description — Piroxicam API Powder (IP / BP / USP / EP)
Piroxicam API Powder is a pharmaceutical-grade active pharmaceutical ingredient (API) supplied as a white to pale yellow crystalline powder with high purity, conforming to major pharmacopeial standards including IP (Indian Pharmacopeia), BP (British Pharmacopeia), USP (United States Pharmacopeia), and EP (European Pharmacopeia). It is widely used by pharmaceutical manufacturers for the formulation of anti-inflammatory, analgesic and pain-relief medicines.
Key Attributes:Chemical Name: Piroxicam (4-Hydroxy-2-methyl-N-(2-pyridinyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide) — NSAID class. CAS Number: 36322-90-4. Molecular Formula: C₁₅H₁₃N₃O₄S, Molecular Weight: ~331.35 g/mol. Appearance: White to off-white or pale yellow crystalline powder. Grade Standards: Complies with IP / BP / USP / EP pharmaceutical specifications. Purity: High-purity API (typically ≥ 99 % on dried basis) with COA and MSDS available. Physical Properties: Practically insoluble in water; freely soluble in organic solvents such as methanol and acetone. Melting Point: Approximately 198–204 °C.
Functional Benefits:Piroxicam API is a non-steroidal anti-inflammatory drug (NSAID) that exhibits analgesic, antipyretic and anti-inflammatory activities. It works by inhibiting the production of prostaglandins — compounds involved in inflammation, pain and swelling — making it a key raw material for arthritis, musculoskeletal pain and related therapeutic formulations.
Packaging & Storage:Packaging: Typically supplied in 25 kg drums or customized bulk packaging with double liners to ensure product integrity. Storage: Store in a cool, dry place, protected from moisture, heat and direct sunlight to maintain stability.

Product Description — Piroxicam API Powder (IP / BP / USP / EP)
Piroxicam API Powder is a pharmaceutical-grade active pharmaceutical ingredient (API) supplied as a white to pale yellow crystalline powder with high purity, conforming to major pharmacopeial standards including IP (Indian Pharmacopeia), BP (British Pharmacopeia), USP (United States Pharmacopeia), and EP (European Pharmacopeia). It is widely used by pharmaceutical manufacturers for the formulation of anti-inflammatory, analgesic and pain-relief medicines.
Key Attributes:Chemical Name: Piroxicam (4-Hydroxy-2-methyl-N-(2-pyridinyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide) — NSAID class. CAS Number: 36322-90-4. Molecular Formula: C₁₅H₁₃N₃O₄S, Molecular Weight: ~331.35 g/mol. Appearance: White to off-white or pale yellow crystalline powder. Grade Standards: Complies with IP / BP / USP / EP pharmaceutical specifications. Purity: High-purity API (typically ≥ 99 % on dried basis) with COA and MSDS available. Physical Properties: Practically insoluble in water; freely soluble in organic solvents such as methanol and acetone. Melting Point: Approximately 198–204 °C.
Functional Benefits:Piroxicam API is a non-steroidal anti-inflammatory drug (NSAID) that exhibits analgesic, antipyretic and anti-inflammatory activities. It works by inhibiting the production of prostaglandins — compounds involved in inflammation, pain and swelling — making it a key raw material for arthritis, musculoskeletal pain and related therapeutic formulations.
Packaging & Storage:Packaging: Typically supplied in 25 kg drums or customized bulk packaging with double liners to ensure product integrity. Storage: Store in a cool, dry place, protected from moisture, heat and direct sunlight to maintain stability.

Guaifenesin API
Product Name: Guaifenesin APICAS No.: 93-14-1. Synonyms: Glyceryl guaiacolate, Guaiacol glyceryl ether, 3-(2-Methoxyphenoxy)-1,2-propanediol. Molecular Formula: C₁₀H₁₄O₄. Molecular Weight: 198.22 g/mol.

Product Overview:
Guaifenesin API is a high-purity active pharmaceutical ingredient widely used in the formulation of expectorant and respiratory therapeutic medicines. It appears as a white to slightly off-white crystalline powder and is manufactured to comply with premium pharmacopeial standards (IP/BP/USP) for pharmaceutical applications. 
Key Specifications:Appearance: White to slightly gray crystalline powder. Assay (Purity): Typically ≥ 99 % (pharma grade). CAS Number: 93-14-1. Molecular Formula: C₁₀H₁₄O₄.Grade: IP / BP / USP (pharmacopeial grade). Physical Form: Powder. Packaging: 25 kg fiber/HDPE drum or customized packaging as per requirement. Storage: Store in a cool, dry, well-ventilated place; protect from moisture and direct light.
Product Features:Pharmaceutical-Grade API: Manufactured under strict quality control, suitable for medicinal use. High Purity & Consistency: Ensures reliable performance in formulations. Comprehensive Documentation: Supplied with COA, MSDS, and regulatory support. Broad Application: Ideal for cough syrup, tablet, capsule and liquid drug production.
Applications:Guaifenesin API is primarily used in the pharmaceutical industry for:Expectorant Medicines: Key API in formulations used to relieve chest congestion and help clear mucus from the respiratory tract. Cough & Cold Products: Incorporated into over-the-counter and prescription cough syrups, tablets and lozenges. Combination Respiratory Therapies: Often used with other antitussives, antihistamines or decongestants in multi-symptom respiratory medicines. Pharmaceutical Manufacturing: Suitable for API suppliers, drug formulators and contract manufacturers.
Handling & Storage:Store Guaifenesin API in tightly closed containers in a cool, dry environment and avoid exposure to moisture, heat and direct sunlight. Follow standard pharmaceutical handling and safety practices when processing and packaging the API.

Tamoxifen Citrate IP – Product Description
Product Name: Tamoxifen CitrateGrade: IP (Indian Pharmacopoeia) / Pharma Grade.CAS Number: 54965-24-1.Molecular Formula: C₂₆H₂₈N₂·C₆H₈O₇ (citrate salt).Molecular Weight: ~563.64 g/mol.Appearance: White to off-white crystalline powder.

Description:
Tamoxifen Citrate IP is a high-quality active pharmaceutical ingredient (API) widely used in the manufacture of antineoplastic (anti-cancer) formulations. It is a selective estrogen receptor modulator (SERM) that plays a key role in hormone-based therapy, particularly in the treatment and prevention of estrogen receptor-positive (ER+) breast cancer. Being compliant with Indian Pharmacopoeia (IP) standards, this API is suitable for regulated domestic and export pharmaceutical formulations.
Key Features & Benefits:Pharmacopoeial Quality: Complies with Indian Pharmacopoeia (IP) standards.High Purity: Consistent assay and quality for reliable formulation performance.SERM Mode of Action: Modulates estrogen receptors to inhibit cancer cell proliferation.Manufacturing Versatility: Suitable for tablets, capsules, and other solid dosage forms.Stable & Process-Friendly: Excellent physical and chemical stability under recommended storage.
Technical Specifications (Typical):Assay (Purity): Meets IP limits for pharmaceutical use.Identification: Conforms to IP identification tests.Impurities: Within IP prescribed limits.Appearance: White to off-white crystalline powder.Solubility: Practically insoluble in water; soluble in organic solvents (as per IP).
Packaging & Storage:Standard Packaging: 25 kg / 50 kg HDPE bags, drums, or custom packaging on request.Storage Conditions: Store in a cool, dry, well-ventilated place, protected from moisture and light.Shelf Life: As per manufacturer specification and IP guidelines.

Tamoxifen Citrate USP
Product Name: Tamoxifen Citrate USP – Pharmaceutical API PowderCAS No.: 54965-24-1.Chemical Name: (Z)-2-[4-(1,2-Diphenyl-1-butenyl)phenoxy]-N,N-dimethylethanamine citrate (1:1).Molecular Formula: C₂₆H₂₉NO · C₆H₈O₇.Molecular Weight: 563.64 g/mol.Appearance: Fine white to off-white crystalline powder.Grade: Pharmaceutical Active Ingredient (API) – USP / BP / EP compliant.Packaging: 5 kg / 10 kg / 25 kg HDPE drums with liners (custom export packaging available).Shelf Life: Up to 2–5 years when stored properly.

Product Description:
Tamoxifen Citrate USP is a high-purity active pharmaceutical ingredient (API) widely used in the formulation of anti-estrogen and oncology drug products. It is a non-steroidal selective estrogen receptor modulator (SERM) that exhibits both estrogenic and anti-estrogenic activity by binding to estrogen receptors in target tissues, making it a cornerstone molecule in hormone-related cancer therapies. Supplied as a fine crystalline powder with consistent physico-chemical properties that meet USP standards, Tamoxifen Citrate API is suitable for development and manufacturing of oral solid dosage forms such as tablets and capsules.
Key Features & Benefits:Pharmaceutical-Grade API: Meets USP (United States Pharmacopeia) purity and quality standards, with regulatory documentation support. High Purity & Consistency: Typically ≥ 99 % assay, ensuring reliable performance in drug formulation and manufacturing. Selective Estrogen Receptor Modulator: Core API for drugs targeting hormone-sensitive conditions. Stable & Easy to Handle: Free-flowing powder suitable for large-scale pharmaceutical production. Broad Compliance: Can meet USP/BP/EP standards depending on customer requirements.
Applications:Tamoxifen Citrate USP API is widely used in:Breast Cancer Therapeutics: API in formulations for adjuvant therapy and metastatic breast cancer treatment. Hormone-Modulating Medications: Used in developing selective estrogen receptor modulators for various clinical indications. Pharmaceutical Manufacturing: Suitable for tablets, capsules, and other solid oral dosage forms. Clinical R&D: Utilized by pharmaceutical researchers for drug development and quality control testing.
Storage & Handling:Store Tamoxifen Citrate USP powder in a cool, dry, and ventilated area, away from moisture and direct sunlight. Protect from heat and light to preserve product quality. Keep containers tightly sealed when not in use. Use proper PPE (gloves, mask, goggles) during handling to avoid dust inhalation and contamination.

Tamoxifen Citrate BP – Product Description
Product Name: Tamoxifen Citrate BPCAS No.: 54965-24-1Chemical Name: (Z)-2-[4-(1,2-Dimethyl-5-phenyl-3-pyrrolidinyl)phenyl]-1,2-ethenediyl]-bis-(dimethylammonium) citrateMolecular Formula: C₂₈H₃₂N₂•C₆H₈O₇Pharmacopoeia Standard: British Pharmacopoeia (BP)Purity: ≥99% (or per customer requirement)Appearance: White to Off-White Crystalline PowderCategory: Pharmaceutical Active Pharmaceutical Ingredient (API).

Product Overview:
Tamoxifen Citrate BP is a high-quality pharmaceutical API widely used in the formulation of anti-estrogen therapies. It is commonly applied in the manufacture of oral dosage forms for the treatment and management of hormone-responsive breast cancer. Supplied as a BP-grade powder, this API meets established compendial standards for purity, identity, and performance.
Key Features & Benefits:BP-Grade Quality: Conforms to British Pharmacopoeia standards for pharmaceutical use.High Purity: Assured chemical purity and minimal impurities for consistent performance.Formulation-Ready: Ideal for tablets, capsules, and other solid oral dosage forms.Reliable Supply: Consistent batch-to-batch quality with comprehensive documentation.Stable & Robust: Good chemical stability under recommended storage conditions.
Packaging Options:1 kg / 5 kg / 10 kg / 25 kg HDPE Bags with Inner PE Liner.Customized packaging available upon request.
Storage & Handling:Store in a cool, dry, and well-ventilated place.Keep container tightly closed.Protect from moisture and direct sunlight.Follow standard pharmaceutical handling and safety guidelines.
Why Choose Us:Trusted supplier with global export experience.Competitive pricing and flexible minimum order quantities (MOQ).Prompt delivery and responsive customer support.Technical and regulatory assistance available for buyers.

Clopidogrel Bisulphate BP
Product Name: Clopidogrel Bisulphate BP – Pharmaceutical Active Ingredient (API):CAS No.: 120202-66-6.Chemical Formula: C₁₆H₁₆ClNO₂S · H₂SO₄.Molecular Weight: 419.90 g/mol.Grade: Pharmaceutical API – British Pharmacopoeia (BP) compliant.Appearance: White to off-white crystalline powder.Packaging: 5 kg / 10 kg / 25 kg HDPE drums with inner liners (custom export packaging available).

Product Description:
Clopidogrel Bisulphate BP API is a high-quality active pharmaceutical ingredient used by pharmaceutical manufacturers in the formulation of antiplatelet cardiovascular medicines. It belongs to the thienopyridine class of antiplatelet agents and acts by irreversibly inhibiting platelet aggregation — reducing the risk of blood clot formation and helping to prevent heart attacks, strokes, and other thrombotic events in patients at risk. This API is supplied as a pure, white to off-white crystalline powder with consistent physical and chemical properties, suitable for use in oral solid dosage forms like tablets, capsules, and other formulations.
Key Features & Benefits:BP-Grade Quality: Complies with British Pharmacopoeia (BP) standards for purity and quality. High Purity & Stability: Typically ≥ 98 % purity with reliable performance for downstream formulation. Broad Therapeutic Use: Used in the manufacture of antiplatelet medicines for cardiovascular diseases. Consistent Physical Properties: Free-flowing powder that supports efficient processing and uniform blending. Pharma Manufacturing Ready: Ideal for use in tablets, capsules, and other oral solid dosage forms.
Applications:Clopidogrel Bisulphate BP API is widely used in:Antiplatelet Drug Manufacturing: Essential API in formulations that prevent blood clot formation in conditions like coronary artery disease, acute coronary syndrome, and peripheral artery disease. Cardiovascular Therapeutics: Helps in producing medicines aimed at reducing the risk of heart attack and stroke. Pharmaceutical R&D: Suitable for research and development of generic and specialty antithrombotic products.
Storage & Handling:Store Clopidogrel Bisulphate BP API in a cool, dry, and well-ventilated area, away from moisture, heat, and direct sunlight. Keep containers tightly closed to preserve quality. Use appropriate PPE (gloves, mask, goggles) when handling to avoid inhalation and contact with fine powder.

Clopidogrel Bisulphate IP
Product Name: Clopidogrel Bisulphate IP – Pharmaceutical APICAS No.: 120202-66-6.Chemical Formula: C₁₆H₁₆ClNO₂S · H₂SO₄.Molecular Weight: 419.9 g/mol.Grade: Pharmaceutical Grade – IP (Indian Pharmacopoeia).Appearance: White to off-white crystalline powder.Packaging: 5 kg / 10 kg / 25 kg HDPE drums with inner liner (custom export packing available).

Product Description:

Clopidogrel Bisulphate IP is a high-quality active pharmaceutical ingredient (API) widely used in the manufacture of antiplatelet cardiovascular medicines. It belongs to the thienopyridine class of antiplatelet agents and works by irreversibly inhibiting platelet aggregation, helping prevent the formation of dangerous blood clots that can lead to heart attacks, strokes, and other thrombotic complications. This API is supplied as a stable, white to off-white crystalline powder with consistent purity and excellent physico-chemical properties, making it ideal for direct use in pharmaceutical formulation of tablets, capsules, or other oral dosage forms. 
Key Features & Benefits:IP-Grade Quality: Manufactured and tested to comply with Indian Pharmacopoeia (IP) standards, ensuring high purity and regulatory compliance. Antiplatelet Action: Helps in preventing platelet clumping by inhibiting the P2Y12 ADP receptor on platelets, reducing risk of clot-related events. Pharma Manufacturing Ready: Suitable for use by pharmaceutical companies in the formulation of cardiovascular therapeutic products. Consistent Quality: Manufactured under GMP conditions with reliable batch-to-batch reproducibility. Comprehensive Documentation: Supplied with Certificate of Analysis (CoA), MSDS, and other regulatory documents on request.
Applications:Clopidogrel Bisulphate IP is widely used in:Cardiovascular Drug Manufacturing: As the key API for antiplatelet medicines used in the prevention of heart attacks and strokes. Dual Antiplatelet Therapy (DAPT): Co-formulations with aspirin or other agents to reduce clotting after stent placement and in acute coronary syndromes. Pharmaceutical Formulations: Ideal for tablets, capsules, and other oral solid dosage forms targeting thrombotic conditions. 
Storage & Handling:Store Clopidogrel Bisulphate IP powder in a cool, dry, and well-ventilated place, away from moisture and direct sunlight. Keep containers tightly closed to maintain product integrity. Use standard PPE (gloves, mask, goggles) while handling to avoid dust exposure.

Guaifenesin USP Powder 
Product Name: Guaifenesin USP Powder / Guaifenesin USP Powder Bulk (Pharmaceutical API)CAS No.: 93-14-1.Chemical Name: 3-(2-Methoxyphenoxy)-1,2-propanediol (Glyceryl guaiacolate).Molecular Formula: C₁₀H₁₄O₄.Molecular Weight: 198.22 g/mol.Grade: Pharmaceutical API – USP / BP / IP compliant.Appearance: White to slightly grey crystalline powder.Packaging: Standard export packaging (e.g., 25 kg HDPE drums w/ liners)Shelf Life: Up to 5 years when stored properly.

Product Description:
Guaifenesin USP Powder is a high-quality active pharmaceutical ingredient (API) widely used in the formulation of expectorant medicines for respiratory health. As an oral expectorant, guaifenesin helps to loosen and thin mucus in the airways, making coughs more productive and aiding in the clearance of phlegm associated with colds, bronchitis, and other respiratory conditions. Supplied as a white to slightly grey crystalline powder with consistent purity and stability, it meets pharmacopeial standards and is suitable for use in tablets, capsules, syrups, and other dosage forms.
Key Features & Benefits:Pharmaceutical-Grade API: Complies with USP / BP / IP monographs, ensuring quality and regulatory acceptance for global markets. Expectorant Action: Used in cough and cold formulations to assist with clearance of respiratory tract mucus. High Purity & Stability: Typically supplied with high assay values and consistent physicochemical properties. Broad Solubility: Soluble in water, alcohol, and other solvents, facilitating formulation flexibility. Reliable Performance: Suitable for pharmaceutical manufacturers, contract formulators, and R&D labs.
Applications:Guaifenesin USP Powder is used in:Antitussive & Expectorant Medicines: Core API for products designed to relieve chest congestion and cough. Respiratory Therapeutics: Included in formulations for bronchitis, sinusitis, flu, and chronic respiratory conditions. Tablets, Capsules & Syrups: Suitable for solid and liquid oral dosage forms. Pharmaceutical R&D: Used in development of new or generic expectorant products.
Storage & Handling:Store Guaifenesin USP Powder in a cool, dry, well-ventilated area, away from moisture and direct sunlight. Keep containers tightly sealed to preserve quality. Use appropriate PPE (gloves, mask, goggles) to prevent inhalation or contact with fine powder during handling.

Clopidogrel Bisulphate USP 
Product Name: Clopidogrel Bisulphate USP (API)CAS No.: 120202-66-6Pharmacopoeia Standard: USP / BP / EP compliant.Molecular Formula: C₁₆H₁₆ClNO₂S · H₂SO₄.Molecular Weight: ~419.9 g/mol.Appearance: White to off-white crystalline powder.Grade: Pharmaceutical Grade API.Packaging: Export-standard packaging (e.g., 1 kg to 25 kg drums).

Product Description:
Clopidogrel Bisulphate USP API is a high-quality active pharmaceutical ingredient used in the manufacture of antiplatelet cardiovascular medicines. It belongs to the thienopyridine class of drugs and is widely used to develop oral antiplatelet formulations that help reduce the risk of heart attacks and strokes by inhibiting platelet aggregation. Clopidogrel Bisulphate is provided as a white to off-white powder with consistent purity and physical properties, suitable for pharmaceutical formulation into tablets, capsules, and other solid oral dosage forms.
Key Features & Benefits:Pharmaceutical-Grade Quality: Manufactured to meet stringent USP standards for global pharmaceutical markets. Antiplatelet API: Essential API for medicines that prevent the formation of blood clots in coronary artery disease, stroke, and peripheral vascular disease. Reliable Performance: Consistent physical and chemical properties ensure reliable batch-to-batch formulation results. Broad Compatibility: Ideal for use in various oral solid dosage manufacturing processes. Comprehensive Testing: Supplied with certificate of analysis (CoA), meeting identification and purity tests by HPLC/IR and other standard methods.
Applications:Clopidogrel Bisulphate USP API is primarily used in:Cardiovascular Therapeutics: Formulation of antiplatelet agents to prevent myocardial infarction (heart attack) and stroke in high-risk patients. Pharmaceutical Manufacturing: Used by pharmaceutical companies as a key API for tablets and capsules targeting platelet aggregation inhibition. Research & Development: Suitable for formulation R&D work in new antithrombotic drug products.
Physical & Chemical Specifications:Appearance: White to off-white crystalline powder. Assay (Purity): Typically 97 – 101.5 % (USP standard). Solubility: Soluble in acidic media and methanol; slight solubility in other organic solvents. Identification: Conforms to standard IR, HPLC, and sulfate tests.
Storage & Handling:Store in a cool, dry, and well-ventilated area away from moisture and direct heat. Keep containers tightly closed to preserve product integrity. Handle with appropriate PPE (gloves, mask, goggles).

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.