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01 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
02 1INDENA S.P.A. Milano IT
03 1JANSSEN PHARMACEUTICA NV Beerse BE
04 1JUBILANT PHARMOVA LIMITED Nanjangud IN
05 1SANOCHEMIA PHARMAZEUTIKA GMBH Neufeld an der Leitha AT
06 1SCINOPHARM TAIWAN, LTD. Shan-Hua TW
07 1Sanochemia Pharmazeutika AG Vienna AT
08 1TAPI CZECH INDUSTRIES S.R.O. Opava CZ
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01 2Galantamine hydrobromide, Isolated from natural sources
02 5Galantamine hydrobromide, Produced by a synthetic process
03 1Galantamine hydrobromide, produced by a synthetic process
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01 2Austria
02 1Belgium
03 2India
04 1Israel
05 1Italy
06 1Taiwan
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01 7Valid
02 1Withdrawn by Holder
Galantamine Hydrobromide, Produced By A Syntheti...
Certificate Number : CEP 2009-316 - Rev 03
Status : Valid
Issue Date : 2024-10-30
Type : Chemical
Substance Number : 2366
Galantamine Hydrobromide, Isolated From Natural ...
Certificate Number : R1-CEP 2011-288 - Rev 01
Status : Valid
Issue Date : 2020-11-19
Type : Chemical
Substance Number : 2366
Galantamine Hydrobromide, Produced By A Syntheti...
Certificate Number : R1-CEP 2012-248 - Rev 01
Status : Valid
Issue Date : 2021-11-19
Type : Chemical
Substance Number : 2366
Galantamine Hydrobromide, Produced By A Syntheti...
Certificate Number : R1-CEP 2011-123 - Rev 02
Status : Valid
Issue Date : 2022-08-12
Type : Chemical
Substance Number : 2366
Galantamine Hydrobromide, Produced By A Syntheti...
Certificate Number : CEP 2023-389 - Rev 00
Status : Valid
Issue Date : 2024-06-19
Type : Chemical
Substance Number : 2366
Galantamine Hydrobromide, Produced By A Syntheti...
Certificate Number : R1-CEP 2012-328 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2019-03-07
Type : Chemical
Substance Number : 2366
Galantamine Hydrobromide, Produced By A Syntheti...
Certificate Number : CEP 2011-011 - Rev 02
Status : Valid
Issue Date : 2024-10-21
Type : Chemical
Substance Number : 2366
Galantamine Hydrobromide, Isolated From Natural ...
Certificate Number : CEP 2011-053 - Rev 03
Status : Valid
Issue Date : 2025-01-13
Type : Chemical
Substance Number : 2366
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PharmaCompass offers a list of Galantamine Hydrobromide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Galantamine Hydrobromide manufacturer or Galantamine Hydrobromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Galantamine Hydrobromide manufacturer or Galantamine Hydrobromide supplier.
PharmaCompass also assists you with knowing the Galantamine Hydrobromide API Price utilized in the formulation of products. Galantamine Hydrobromide API Price is not always fixed or binding as the Galantamine Hydrobromide Price is obtained through a variety of data sources. The Galantamine Hydrobromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nivalin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nivalin, including repackagers and relabelers. The FDA regulates Nivalin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nivalin 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 Nivalin supplier is an individual or a company that provides Nivalin active pharmaceutical ingredient (API) or Nivalin finished formulations upon request. The Nivalin suppliers may include Nivalin API manufacturers, exporters, distributors and traders.
click here to find a list of Nivalin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nivalin CEP of the European Pharmacopoeia monograph is often referred to as a Nivalin Certificate of Suitability (COS). The purpose of a Nivalin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Nivalin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Nivalin to their clients by showing that a Nivalin CEP has been issued for it. The manufacturer submits a Nivalin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Nivalin CEP holder for the record. Additionally, the data presented in the Nivalin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Nivalin DMF.
A Nivalin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Nivalin CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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