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Bulk Drugs APIs
We are a leading Exporter of meloxicam api powder ip/bp/usp/ep, lidocaine hcl bp, diphenhydramine hcl ip, letrozole api powder, chlorhexidine gluconate solution and ambroxol hcl ip from Ahmedabad, India.
Meloxicam Api Powder IP/BP/USP/EP
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Rs 999 / KgPrice on Request
Product Brochure
| Purity | Greater than 99% |
| Packaging Type | Drum |
| Manufacturer | yes |
| Country of Origin | Made in India |
| Grade Standard | IP/BP/USP/EP |
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.
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Lidocaine Hcl Bp
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Rs 800 / KgPrice on Request
Product Brochure
| Grade Standard | BP |
| Packaging Type | Bag |
| Packaging Size | 25 kg |
| Form | Powder |
| CAS NO | 137-58-6 |
| Chemical Formula | C14H22N2O |
| Molecular Weight | 234.34 g/mol |
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.
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Diphenhydramine HCL IP
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Rs 99 / KgPrice on Request
Product Brochure
| Grade Standard | IP |
| Packaging Type | Bag |
| Packaging Size | 25 kg |
| CAS NO | 58-73-1 |
| Chemical Formula | C17H21NO |
| Molecular Weight | 255.355 g/mol |
Product Name: Diphenhydramine HCl IP – Pharmaceutical Active Ingredient (API)CAS No.: 147-24-0.Chemical Name: Diphenhydramine Hydrochloride (2-Diphenylmethoxy-N,N-dimethylethanamine hydrochloride).Grade: Pharmaceutical / API – Indian Pharmacopoeia (IP).Appearance: White to off-white crystalline powder.Molecular Formula: C₁₇H₂₂ClNO · HCl.Molecular Weight: 291.82 g/mol.Packaging: 5 kg / 10 kg / 25 kg HDPE drums with inner liners (custom export packaging available).
Product Description:
Diphenhydramine HCl IP is a high-quality active pharmaceutical ingredient (API) widely used in the formulation of antihistamine and related therapeutic medicines. It is a first-generation H₁ receptor antagonist that helps inhibit the effects of endogenous histamine, which plays a central role in allergic reactions. Supplied as a white to off-white crystalline powder with consistent physicochemical properties, this API is suitable for use in oral, topical, and other dosage form formulations by licensed pharmaceutical manufacturers.
Key Features & Benefits:IP-Grade Quality: Conforms to Indian Pharmacopoeia (IP) standards for purity and quality, ensuring regulatory compliance and consistent performance in formulations. High Purity: Typically supplied with ≥ 98 % purity, meeting industry expectations for API use. Effective Antihistamine API: Blocks the action of histamine at H₁ receptor sites, making it an essential ingredient in anti-allergy medications. Stable & Reliable: Supplied as a stable compound with predictable handling and formulation behavior. Documentation Available: Certificate of Analysis (CoA), MSDS, and regulatory documentation can be provided on request.
Applications:Diphenhydramine HCl IP API is widely used in the pharmaceutical industry for:Antihistamine Medicine Manufacturing: Core API for producing medicines used to relieve symptoms of allergic rhinitis, hay fever, and other allergic conditions. Cold & Allergy Products: Used in formulations that help manage coughs, runny nose, sneezing, and itching associated with the common cold and allergies. Sedative & Sleep Aid Formulations: Due to its sedative properties, it can be included in products intended for short-term management of insomnia and motion sickness (where permitted). Pharmaceutical R&D: Suitable for research and development of generics and specialty antihistamine products.
Storage & Handling:Store Diphenhydramine HCl IP in a cool, dry, and well-ventilated area, away from moisture and direct sunlight. Keep containers tightly sealed to preserve quality. Use appropriate PPE (gloves, mask, goggles) to minimize dust exposure during handling.
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Letrozole API Powder
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Rs 99 / KgPrice on Request
Minimum Order Quantity: 10 Kg
Product Brochure
| Grade Standard | Pharma Grade |
| Purity | Greater than 99% |
| Bulk Density | 1.21g/cm3 |
| Chemical Formula | C17H11N5 |
| Molecular Weight | 285.31 g/mol |
| Usage/Application | Pharmaceutical Intermediates,Syntheses Material Intermediates |
| Form | Powder |
Product Name: LetrozoleSynonyms: Letrozol, 4,4′-(1H-1,2,4-triazol-1-ylmethylene) bisbenzonitrileCAS Number: 112809-51-5Molecular Formula: C₁₇H₁₁N₅Molecular Weight: 285.30 g/mol
Description:
Letrozole API Powder is a high-purity pharmaceutical active ingredient supplied as a white to off-white crystalline powder designed for use in the formulation of hormone therapy medications. It is a third-generation non-steroidal aromatase inhibitor, widely used in the treatment of hormonally-responsive breast cancer in postmenopausal women and other therapeutic applications. The product is manufactured under strict quality standards and is suitable for incorporation into solid dosage forms such as tablets and capsules.
Key Features & Benefits:Pharmaceutical-Grade API: High purity (typically ≥99%) meeting USP/EP/BP pharmacopoeial specifications for pharmaceutical manufacturing. Consistent Quality: Physicochemical properties optimized for reliable formulation performance and regulatory compliance. Potent Aromatase Inhibitor: Inhibits the aromatase enzyme, reducing estrogen synthesis — essential for estrogen-dependent cancer therapies. Stable and Well-Characterized: Produced with comprehensive analytical documentation (COA) and consistent batch-to-batch quality. Versatile API: Ideal for oncology drug manufacturers, contract formulators, and research laboratories.
Typical Specifications (Indicative):Appearance: White to off-white crystalline powder Assay (Purity): ≥99.0% (HPLC, USP/EP grade) Melting Point: Approx. 181–185 °C pH (1% Solution): ~5.0-7.0 Solubility: Slightly soluble in water, soluble in organic solvents.
Packaging Options:1 kg / 5 kg Bottles or Drums (with inner liners).10 kg / 25 kg Export-worthy HDPE Drums.Customized packaging options as per client requirements.
Storage & Handling:Store in a cool, dry, and well-ventilated place away from direct sunlight, moisture, or heat. Handle with appropriate protective equipment and follow standard pharmaceutical API handling procedures.
Why Choose Our Letrozole API Powder?We offer premium quality Letrozole API with consistent purity, strict quality control, and comprehensive documentation to support regulatory filings and manufacturing needs. Our product is ideal for pharmaceutical companies, formulation specialists, and contract manufacturers seeking a reliable active ingredient for oncology drug production.
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Chlorhexidine Gluconate Solution
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Rs 99 / KgPrice on Request
Product Brochure
| Form | Liquid |
| Molecular Formula | C22H30Cl2N10 |
| CAS NO | 55-56-1 |
| Molar Mass | 505.446 g/mol |
| Solubility in Water | 0.8 kg/m3 |
| Melting Point | 134 to 136 deg C (273 to 277 deg F) |
Product Name: Chlorhexidine Gluconate Solution (20% w/v)CAS No.: 18472-51-0Grade: IP / BP / USP (Pharmaceutical & Industrial Grade).
Product Overview:
Chlorhexidine Gluconate Solution is a broad-spectrum antiseptic and disinfectant liquid widely used in pharmaceutical, personal care, healthcare, and hygiene applications. It is a bisbiguanide antimicrobial compound effective against a wide variety of gram-positive and gram-negative bacteria, some yeasts, and microorganisms.
Chemical & Physical Properties:Chemical Name: Chlorhexidine Gluconate (also known as Chlorhexidine Digluconate). Molecular Formula: C34H54Cl2N10O14. Molecular Weight: ~897.7 g/mol. Appearance: Clear, colorless to pale yellow liquid. Concentration: 19–21% w/v (commonly 20%). pH: ≈5.5 – 7.0. Density: ~1.06–1.07 g/mL. Solubility: Miscible with water; soluble in alcohols and acetone.
Key Features & Advantages:Broad-spectrum antimicrobial action against bacteria and fungi. Suitable for hospital, clinical, and personal care formulations. Stable liquid form for easy formulation and dosing. Meets pharmacopoeial standards (IP/BP/USP). Long shelf life when stored under recommended conditions.
Applications:Chlorhexidine Gluconate Solution is used as:Antiseptic disinfectant for skin, hands, and wound care in healthcare settings. Preservative and biocide in personal care products, cleansers, and soaps. Active ingredient in oral hygiene formulations such as mouthwashes and rinses (in low concentrations). Sanitizer and hygiene solution for surfaces and equipment cleaning. Raw material for pharmaceutical product manufacturing and topical formulations.
Safety & Handling:For external use / industrial use only — not for direct ingestion.Wear appropriate PPE (gloves, goggles) when handling.Store in a cool, dry, ventilated place, away from direct sunlight and heat. Avoid contact with eyes and skin; in case of contact, rinse thoroughly.
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Ambroxol HCL IP
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Price on Request
Product Brochure
| Packaging Type | Bag |
| Purity | 99% |
| Grade Standard | IP |
| CAS NO | 18683-91-95 |
| Chemical Formula | C13H18Br2N2O |
| Molecular Weight | 378.10 g/mol |
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
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White powder Piroxicam BP
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Rs 99 / KgPrice on Request
Product Brochure
| Grade Standard | Technical Grade |
| Physical State | Powder |
| Packaging Size | 25 kg |
| Purity | 99% |
| Packaging Type | Bag |
| Color | White |
| Molecular Formula | C15H13N3O4S |
Product Name: Piroxicam BPSynonyms / Chemical Name: 4-Hydroxy-2-methyl-N-(2-pyridinyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide, Piroxicam, Feldene APICAS No.: 36322-90-4 Molecular Formula: C₁₅H₁₃N₃O₄S Molecular Weight: ~331.35 g/mol Appearance: White to off-white crystalline powder (BP quality) Grade: British Pharmacopoeia (BP) Pharmaceutical API.
Product Description:
Piroxicam BP is a high-purity non-steroidal anti-inflammatory drug (NSAID) active pharmaceutical ingredient supplied as a white to slightly yellow crystalline powder. It is manufactured to British Pharmacopoeia (BP) standards, ensuring quality, consistency and suitability for pharmaceutical formulation use. Piroxicam is widely used in anti-inflammatory, analgesic and pain-relief medications designed to treat conditions such as arthritis, musculoskeletal pain and inflammatory disorders.
Key Features:BP Pharmacopeial API: Conforms to British Pharmacopoeia quality and assay standards. White to off-white powder: Fine crystalline form for easy handling and formulation. High purity: Suitable for pharmaceutical manufacturers producing tablets, capsules or other dosage forms. Reliable performance: Consistent physical characteristics and stability for downstream processing. Essential NSAID API: Used for managing pain, inflammation and related symptoms.
Typical Physical & Chemical Properties:Appearance: White to off-white crystalline powder. Solubility: Practically insoluble in water; soluble in methylene chloride; slightly soluble in anhydrous ethanol. Melting Point: ~198 – 200 °C (typical) Assay / Purity: Typically ≥ 98.5 % on dried basis as per BP limits. Storage: Store in a cool, dry place, protected from light.
Applications:Pharmaceutical Manufacturing: API for analgesic and anti-inflammatory finished products. Prescription Medicine Formulations: Used in tablets, capsules and other oral forms for pain and inflammation relief. API Supply: Reliable source of BP-grade piroxicam for formulation houses and bulk drug producers.Packaging & Storage:Typically supplied in 25 kg HDPE or fibre drums with protective liners on request. Store in a cool, dry environment away from moisture and direct sunlight to maintain product integrity.
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Guaifenesin USP Powder
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Rs 99 / KgPrice on Request
Product Brochure
| Grade Standard | USP |
| Packaging Size | 25 kg |
| Physical State | Powder |
| Packaging Type | Bag, Drum |
| Molecular Weight | 198.216 g/mol |
| Chemical Formula | C10H14O4 |
| CAS NO | 93-14-1 |
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.
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Glibenclamide Api Powder IP/BP/USP/EP
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Rs 99 / KgPrice on Request
Product Brochure
| Purity | Greater than 99% |
| Country of Origin | Made in India |
| Packaging Type | Drum |
| Colour | White |
| Grade Standard | IP/BP/USP/EP |
Product Name: Glibenclamide API PowderSynonyms: Glyburide.CAS No.: 10238-21-8.Grade: IP / BP / USP (Medicine Grade).
Product Overview:
Glibenclamide API Powder is a high-quality active pharmaceutical ingredient (API) primarily used in the manufacture of oral antidiabetic medications. It belongs to the sulfonylurea class of hypoglycemic agents and plays a key role in controlling blood glucose levels in patients with type 2 diabetes mellitus by stimulating insulin release from pancreatic β-cells.
Chemical & Physical Properties:Chemical Name: 5-chloro-N-[2-[4-(cyclohexylcarbamoylsulfamoyl)phenyl]ethyl]-2-methoxybenzamide. Molecular Formula: C23H28ClN3O5S. Molecular Weight: ≈ 494.00 g/mol. Appearance: White or almost white crystalline powder.Purity: ≥98 % (HPLC) typical (varies by supplier). Melting Point: ~169–174 °C.Solubility: Practically insoluble in water; sparingly soluble in organic solvents such as ethanol, methanol, and chloroform.
Key Features & Benefits:Pharmaceutical-grade API suitable for finished drug formulations. High chemical purity and consistency, meeting international pharmacopeial standards (USP/BP/IP). Stable crystalline powder form for easy handling, formulation, and processing. Comprehensive Quality Documentation (COA, MSDS) available upon request (depends on supplier). Long shelf life when stored under recommended conditions.
Pharmaceutical Application:Glibenclamide API Powder is widely used in the pharmaceutical industry for the manufacture of oral hypoglycemic drugs designed to manage type 2 diabetes mellitus (non-insulin dependent diabetes). It helps regulate elevated blood glucose levels by enhancing insulin secretion from the pancreas.
Usage & Handling:Intended for pharmaceutical manufacturing and R&D use only (not for direct human consumption without formulation). Store in a cool, dry place, away from moisture, heat, and direct sunlight. Follow regulatory and safety standards during handling and storage.
Packaging & Supply Options:Standard packaging: 25 kg drums with inner liners or as per customer requirement. MOQ and pricing vary based on quantity ordered, grade specifications, and delivery terms. Technical support with documents such as COA, MSDS, and quality certificates available on request.
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Bronopol api Powder
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Rs 99 / KgPrice on Request
Product Brochure
| Grade Standard | Reagent Grade |
| Form | Powder |
| Physical State | Powder |
| Packaging Type | Drum |
| Type | Systemic |
| Usage/Application | Laboratory |
| Country of Origin | Made in India |
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.
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Clopidogrel Bisulphate USP
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Rs 999 / KgPrice on Request
Product Brochure
| Grade Standard | USP |
| Prescription/Non prescription | Non prescription |
| Packaging Size | 25 kg |
| Purity | 99% |
| Packaging Type | Bag |
| Form | Powder |
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).
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Sodium Valproate Api
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Rs 99 / KgPrice on Request
Product Brochure
| Grade Standard | IP/BP/USP/EP |
| Purity | Greater than 99% |
| Country of Origin | Made in India |
| Packaging | Drum |
| Form | Powder |
Product Name: Sodium Valproate APICAS No: 1069-66-5Molecular Formula: C₈H₁₅NaO₂Molecular Weight: 166.19 g/mol.
Product Overview:
Sodium Valproate is a pharmaceutical-grade active pharmaceutical ingredient (API) widely used in the manufacture of antiepileptic and mood-stabilizing drug formulations. It appears as a white to off-white crystalline powder with high purity and excellent stability, making it ideal for pharmaceutical processing and formulation.
Key Specifications:Appearance: White crystalline powder.Assay: ≥ 98 % (as per IP/BP/USP standards).CAS Number: 1069-66-5.Grade: IP / BP / USP.Solubility: Soluble in water and ethanol.Packaging: Export standard HDPE/drum or as per customer requirement.Storage: Store in a cool, dry place away from moisture and light.
Product Features:High-quality API with consistent pharmaceutical-grade purity.Complies with international pharmacopeia standards (IP/BP/USP).Supplied with COA (Certificate of Analysis) and MSDS.Suitable for large-scale commercial manufacturing.Ideal for formulators, contract manufacturers, and exporters.
Applications:Sodium Valproate API is predominantly used in the pharmaceutical industry for:Antiepileptic Drug Manufacturing: Core ingredient in tablets, capsules, and liquids for treating various seizure types including generalized, partial, and absence seizures. Mood Stabilizer Formulations: Used in products for bipolar disorder and mania management. Migraine Prophylaxis Medicines: Incorporated in formulations aimed at preventing migraine headaches. Pharma Formulations: Widely used in both adult and pediatric antiepileptic and neuropsychiatric products.
Why Choose Our Sodium Valproate API:Consistent Quality: Manufactured under stringent quality control and GMP principles. Reliable Supply: Available in bulk with customizable packaging and documentation support. Regulatory Support: Comes with complete specification documents, facilitating regulatory compliance and export requirements.
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