01 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
02 1HETERO DRUGS LIMITED Hyderabad IN
03 1SIEGFRIED EVIONNAZ SA Evionnaz CH
04 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
01 4Fosinopril sodium
01 1China
02 2India
03 1Switzerland
01 4Valid
Certificate Number : CEP 2010-030 - Rev 02
Status : Valid
Issue Date : 2023-12-06
Type : Chemical
Substance Number : 1751
Certificate Number : CEP 2013-018 - Rev 02
Status : Valid
Issue Date : 2023-11-29
Type : Chemical
Substance Number : 1751
Certificate Number : CEP 2021-425 - Rev 00
Status : Valid
Issue Date : 2024-06-21
Type : Chemical
Substance Number : 1751
Certificate Number : R1-CEP 2011-271 - Rev 01
Status : Valid
Issue Date : 2022-01-11
Type : Chemical
Substance Number : 1751
A FOSINOPRIL SODIUM manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of FOSINOPRIL SODIUM, including repackagers and relabelers. The FDA regulates FOSINOPRIL SODIUM manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. FOSINOPRIL SODIUM 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 FOSINOPRIL SODIUM manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A FOSINOPRIL SODIUM supplier is an individual or a company that provides FOSINOPRIL SODIUM active pharmaceutical ingredient (API) or FOSINOPRIL SODIUM finished formulations upon request. The FOSINOPRIL SODIUM suppliers may include FOSINOPRIL SODIUM API manufacturers, exporters, distributors and traders.
click here to find a list of FOSINOPRIL SODIUM suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A FOSINOPRIL SODIUM CEP of the European Pharmacopoeia monograph is often referred to as a FOSINOPRIL SODIUM Certificate of Suitability (COS). The purpose of a FOSINOPRIL SODIUM CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of FOSINOPRIL SODIUM EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of FOSINOPRIL SODIUM to their clients by showing that a FOSINOPRIL SODIUM CEP has been issued for it. The manufacturer submits a FOSINOPRIL SODIUM CEP (COS) as part of the market authorization procedure, and it takes on the role of a FOSINOPRIL SODIUM CEP holder for the record. Additionally, the data presented in the FOSINOPRIL SODIUM CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the FOSINOPRIL SODIUM DMF.
A FOSINOPRIL SODIUM CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. FOSINOPRIL SODIUM CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of FOSINOPRIL SODIUM suppliers with CEP (COS) on PharmaCompass.
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