01 1M/s Jubilant Pharmova Limited
02 1M/s. Aurobindo Pharma Ltd., (Unit-XI),
01 1Galantamine Hydrobromide (IH)
02 1Galantamine Hydrobromide (Ph.Eur)
01 1WC-0023
02 1WC-0092
01 2India
Galantamine Hydrobromide (Ph.Eur)
Date of Issue : 2019-06-26
Valid Till : 2022-06-25
Written Confirmation Number : WC-0023
Address of the Firm : Sy.No.1/22, 2/1 To 5, 6 to 18, 61 to 69, Pydibhimavaram Village, Ranasthalam, Sr...
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 Galantamine Hydrobromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Galantamine Hydrobromide, including repackagers and relabelers. The FDA regulates Galantamine Hydrobromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Galantamine 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 Galantamine Hydrobromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Galantamine Hydrobromide supplier is an individual or a company that provides Galantamine Hydrobromide active pharmaceutical ingredient (API) or Galantamine Hydrobromide finished formulations upon request. The Galantamine Hydrobromide suppliers may include Galantamine Hydrobromide API manufacturers, exporters, distributors and traders.
click here to find a list of Galantamine Hydrobromide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Galantamine Hydrobromide written confirmation (Galantamine Hydrobromide WC) is an official document issued by a regulatory agency to a Galantamine Hydrobromide manufacturer, verifying that the manufacturing facility of a Galantamine Hydrobromide active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Galantamine Hydrobromide APIs or Galantamine Hydrobromide finished pharmaceutical products to another nation, regulatory agencies frequently require a Galantamine Hydrobromide WC (written confirmation) as part of the regulatory process.
click here to find a list of Galantamine Hydrobromide suppliers with Written Confirmation (WC) on PharmaCompass.
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