Camylofine Dihydrochloride API Manufacturer & Supplier in India

Camylofine Dihydrochloride is a pharmaceutical-grade Active Pharmaceutical Ingredient (API) classified as a Antispasmodic. Hydrochloride salt of camylofine. Mediocon Inc supplies high-purity Camylofine Dihydrochloride API conforming to IP / BP / EP / USP specifications from our GMP-certified manufacturing facility in Aurangabad, Maharashtra, India.

Our Camylofine Dihydrochloride API undergoes stringent quality control testing including assay, related substances, residual solvents, heavy metals, and microbial limits before release. Each batch is accompanied by a full Certificate of Analysis and regulatory documentation.

Key Features

• High-purity pharmaceutical grade API
• IP / BP / EP / USP pharmacopoeial compliance
• Full CoA, MSDS/SDS, and COO documentation per batch
• GMP-certified manufacturing facility in Aurangabad, Maharashtra
• Consistent batch-to-batch quality with HPLC verification
• Export-ready packaging: 25 kg HDPE drums / aluminium foil bags

Why Choose Mediocon

• ISO 9001:2015 & WHO-GMP certified manufacturing
• Export to 40+ countries worldwide
• Flexible MOQ: 1 kg (R&D sample) to 500+ kg commercial lots
• Dedicated QA team for regulatory filings (US FDA, EMA, TGA)
• Competitive pricing with short lead times from Aurangabad facility
• Full regulatory support: DMF, CEP/EDMF on request

Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We supply Camylofine Dihydrochloride and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

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 compliance; all state licensing documentation provided

Quality & Compliance

• ISO 9001:2015 certified quality management system
• WHO-GMP certified manufacturing facility, Aurangabad, Maharashtra
• Full batch traceability — raw material to finished API
• Stability data available (ICH Q1A guidelines) for regulatory submissions
• Microbiological testing per USP <61> / <62> / BP 2.6.12