Pemirolast — CAS 69372-19-6 API Manufacturer & Supplier in India

Pemirolast is a high-purity Active Pharmaceutical Ingredient (API) classified as an Antiallergic agent and Mast Cell Stabilizer. Mediocon Inc manufactures GMP-compliant Pemirolast at its state-of-the-art facility in Aurangabad, Maharashtra, India, supplying pharmaceutical companies worldwide. Pemirolast inhibits the release of chemical mediators from mast cells, making it highly effective in allergic and inflammatory conditions including allergic conjunctivitis.

• Allergic conjunctivitis treatment and prevention
• Mast cell stabilization in ocular allergy
• Seasonal and perennial allergic rhinitis adjunct therapy
• Asthma prophylaxis via mediator release inhibition

• GMP Certified manufacturing facility in Aurangabad, Maharashtra, India
• Full pharmacopoeial compliance: IP / BP / EP / USP standards
• Complete documentation: Certificate of Analysis (CoA), MSDS, Certificate of Origin
• Stringent in-process quality control at every manufacturing stage
• HPLC purity testing and spectroscopic identification (IR, NMR)
• Cold-chain and controlled-environment storage facilities available
• Exported to 40+ countries with full regulatory support

Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Pemirolast — CAS 69372-19-6 (CAS 69372-19-6) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Pemirolast — CAS 69372-19-6 is manufactured under strict quality management protocols compliant with WHO-GMP, ISO 9001:2015, and major pharmacopoeial standards (IP, BP, USP, EP). Every batch undergoes full analytical testing — identity (IR/HPLC), assay, related substances, residual solvents (ICH Q3C), heavy metals, and microbial limits — before release with a Certificate of Analysis.

Export Markets

• USA — FDA-registered facility; DMF support available for ANDA/NDA filings
• Europe — EMA-compliant documentation; CEP/EDMF support on request
• Africa & Middle East — WHO-GMP certified; competitive pricing for emerging markets
• Southeast Asia — established logistics network; temperature-controlled shipments
• India domestic — schedule H/X compliance; all state licensing documentation provided

Quality & Compliance

• ISO 9001:2015 certified quality management system
• GMP-certified manufacturing facility, Aurangabad, Maharashtra
• Full batch traceability from raw material to finished API
• Stability data available (ICH Q1A guidelines) for regulatory submissions
• Dedicated QA team for customer audits and regulatory queries