Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
01 1M/s Rusan Pharma Ltd
02 1M/s M/s. Pioneer Agro Industries Sanvin Laboratories Private Limited
03 1M/s Sun Pharmaceuticals Industries ltd
Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
Buprenorphine Hydrochloride Ph Eur/BP/USP
Date of Issue : 2025-02-11
Valid Till : 2027-06-09
Written Confirmation Number : WC-0278
Address of the Firm : Plot No.6406, 6407 & 6411, GIDC Estate, Ankleshwar-393002, Dist- Bharuch
88
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A BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE, including repackagers and relabelers. The FDA regulates BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE supplier is an individual or a company that provides BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE active pharmaceutical ingredient (API) or BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE finished formulations upon request. The BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE suppliers may include BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE API manufacturers, exporters, distributors and traders.
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A BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE written confirmation (BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE WC) is an official document issued by a regulatory agency to a BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE manufacturer, verifying that the manufacturing facility of a BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE APIs or BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE finished pharmaceutical products to another nation, regulatory agencies frequently require a BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE WC (written confirmation) as part of the regulatory process.
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