Remedy Labs

Olanzapine API Powder
Product Name: Olanzapine API PowderCAS No: 132539-06-1. Grade: Pharmaceutical / Medicine Grade (IP/BP/USP available).

Product Overview:
Olanzapine API Powder is a high-quality active pharmaceutical ingredient (API) used as a key raw material in the manufacture of antipsychotic medications. It belongs to the class of atypical antipsychotic agents, specifically formulated for use in mental health pharmaceutical products. 
Chemical & Physical Properties:Chemical Name: 2-Methyl-4-(4-methyl-1-piperazinyl)-10H-thieno[2,3-b][1,5]benzodiazepine. Molecular Formula: C17H20N4S. Molecular Weight: 312.43 g/mol. Appearance: White to pale yellow crystalline powder. Purity: Typically ≥ 98% (or as specified).Solubility: Practically insoluble in water, freely soluble in organic solvents like chloroform/dichloromethane; slightly soluble in alcohols. Melting Point: Approx. 195 °C. Odor: Odorless or very mild.
Key Features & Benefits:High-Purity Pharmaceutical Grade API for formulation and manufacturing. Consistent Quality — manufactured under stringent quality and regulatory standards (ISO/COA/MSDS/GMP where applicable). Stable Powder Form — easy to handle and formulate for further processing in finished dosage forms. Long Shelf Life and Storage Stability when kept in controlled conditions.
Pharmaceutical Application:Olanzapine API is widely used in the production of antipsychotic medicines for mental health conditions, including:Schizophrenia.Bipolar disorder.Mixed or manic episodes associated with mood disorders.
Usage & Handling:For pharmaceutical manufacturing and laboratory use only.Keep in a cool, dry place, away from moisture, heat, and direct sunlight. Follow all applicable regulatory standards and safety practices during handling.
Packaging & Supply Options:Available in drums, HDPE bags, or customized packaging as per client requirements.MOQ (Minimum Order Quantity) and pricing depend on order volume, grade specifications, and delivery terms.Technical support available including COA, MSDS, and quality documentation on request.

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. 

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.