Remedy Labs

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

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

Furosemide API Powder
Product Type: Active Pharmaceutical Ingredient (API)Chemical Name: FurosemideDosage Form: PowderAppearance: White to off-white crystalline powderGrade: Pharmaceutical GradeCAS No.: 54-31-9Molecular Formula: C₁₂H₁₁ClN₂O₅SMolecular Weight: 330.74 g/mol
Product Description
Furosemide API is a potent loop diuretic widely used in the pharmaceutical industry for the formulation of oral and injectable dosage forms. It is primarily prescribed for the treatment of edema associated with congestive heart failure, liver cirrhosis, renal disorders, and hypertension.
Our Furosemide API Powder is manufactured under strict GMP-compliant conditions to ensure high purity, consistent quality, and excellent stability. It meets pharmacopeial standards and is suitable for use in regulated as well as semi-regulated markets.
Key Features
High purity and consistent quality
Manufactured as per GMP guidelines
Excellent stability and shelf life
Suitable for oral solid and injectable formulations
Reliable documentation support (COA, MSDS)
Applications
Used in the formulation of tablets and injections
Widely applied in diuretic and antihypertensive medicines
Suitable for cardiovascular and renal therapeutic products
Packaging Details
HDPE drums with double LDPE inner lining
Custom packaging available as per client requirement
Storage Conditions
Store in a cool, dry place
Protect from light and moisture
Manufacturer & Supplier
Company Name: Remedy LabsLocation: Ahmedabad, Gujarat, IndiaBusiness Type: Leading Manufacturer of API & Intermediates
Why Choose Remedy Labs?
GMP-compliant manufacturing facility
Strict quality control systems
Competitive pricing
Timely delivery and global supply capability

Metoprolol Succinate API Powder
Product Type: Active Pharmaceutical Ingredient (API)Chemical Name: Metoprolol SuccinateDosage Form: PowderAppearance: White to off-white crystalline powderGrade: Pharmaceutical GradeCAS No.: 98418-47-4Molecular Formula: C₁₈H₂₈N₂O₅Molecular Weight: 356.42 g/mol
Product Description
Metoprolol Succinate API is a selective beta-1 adrenergic receptor blocker widely used in the pharmaceutical industry for the manufacture of extended-release oral solid dosage forms. It is primarily indicated for the treatment of hypertension, angina pectoris, heart failure, and other cardiovascular disorders.
Manufactured under stringent quality standards, our Metoprolol Succinate API Powder offers consistent quality, high purity, and excellent stability, making it suitable for regulated and non-regulated markets.
Key Features
High purity and consistent batch-to-batch quality
Suitable for sustained / extended-release formulations
Manufactured in compliance with GMP guidelines
Stable physicochemical properties
Reliable supply and documentation support
Applications
Used in the formulation of tablets and capsules
Widely applied in cardiovascular drug manufacturing
Suitable for controlled-release pharmaceutical products
Packaging Details
HDPE drums with double LDPE inner lining
Customized packaging available as per customer requirement
Storage Conditions
Store in a cool, dry place
Protect from moisture and direct sunlight
Manufacturer & Supplier
Company Name: Remedy LabsLocation: Ahmedabad, Gujarat, IndiaBusiness Type: Leading Manufacturer of API & Intermediates
Why Choose Remedy Labs?
GMP-compliant manufacturing facility
Strict quality control and documentation
Competitive pricing
Timely delivery and global supply capability