Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
01 2M/s Rusan Pharma Ltd
01 1Nalbuphine Base IH
02 1Nalbuphine Hydrochloride Monohydrate IH
01 2WC-0278
01 2India
Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
Nalbuphine Hydrochloride Monohydrate IH
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
Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
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
85
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A NALBUFINE HYDROCHLORIDE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NALBUFINE HYDROCHLORIDE, including repackagers and relabelers. The FDA regulates NALBUFINE HYDROCHLORIDE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NALBUFINE 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 NALBUFINE HYDROCHLORIDE supplier is an individual or a company that provides NALBUFINE HYDROCHLORIDE active pharmaceutical ingredient (API) or NALBUFINE HYDROCHLORIDE finished formulations upon request. The NALBUFINE HYDROCHLORIDE suppliers may include NALBUFINE HYDROCHLORIDE API manufacturers, exporters, distributors and traders.
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A NALBUFINE HYDROCHLORIDE written confirmation (NALBUFINE HYDROCHLORIDE WC) is an official document issued by a regulatory agency to a NALBUFINE HYDROCHLORIDE manufacturer, verifying that the manufacturing facility of a NALBUFINE HYDROCHLORIDE active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting NALBUFINE HYDROCHLORIDE APIs or NALBUFINE HYDROCHLORIDE finished pharmaceutical products to another nation, regulatory agencies frequently require a NALBUFINE HYDROCHLORIDE WC (written confirmation) as part of the regulatory process.
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