01 1Divi’s Laboratories
02 1M/s Jubilant Pharmova Limited
01 1Bupropion HCI (USP)
02 1Bupropion Hydrobromide USP
01 1WC-0030
02 1WC-0092
01 2India
Date of Issue : 2019-06-17
Valid Till : 2022-06-16
Written Confirmation Number : WC-0030
Address of the Firm : Unit-II, Annavaram(Post), Chippada Village, Beemunipatnam Mandal, Visakhapatan...
Date of Issue : 2022-09-01
Valid Till : 2024-11-04
Written Confirmation Number : WC-0092
Address of the Firm : Plot No. 18, 56, 57 & 58, K.I.A.D.B. Industrial Area\r\nNanjangud - 571 302, Mys...
A Bupropion Hydrobromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bupropion Hydrobromide, including repackagers and relabelers. The FDA regulates Bupropion Hydrobromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bupropion Hydrobromide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Bupropion Hydrobromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bupropion Hydrobromide supplier is an individual or a company that provides Bupropion Hydrobromide active pharmaceutical ingredient (API) or Bupropion Hydrobromide finished formulations upon request. The Bupropion Hydrobromide suppliers may include Bupropion Hydrobromide API manufacturers, exporters, distributors and traders.
click here to find a list of Bupropion Hydrobromide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Bupropion Hydrobromide written confirmation (Bupropion Hydrobromide WC) is an official document issued by a regulatory agency to a Bupropion Hydrobromide manufacturer, verifying that the manufacturing facility of a Bupropion Hydrobromide active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Bupropion Hydrobromide APIs or Bupropion Hydrobromide finished pharmaceutical products to another nation, regulatory agencies frequently require a Bupropion Hydrobromide WC (written confirmation) as part of the regulatory process.
click here to find a list of Bupropion Hydrobromide suppliers with Written Confirmation (WC) on PharmaCompass.
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