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 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fosinopril, including repackagers and relabelers. The FDA regulates Fosinopril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fosinopril 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 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fosinopril supplier is an individual or a company that provides Fosinopril active pharmaceutical ingredient (API) or Fosinopril finished formulations upon request. The Fosinopril suppliers may include Fosinopril API manufacturers, exporters, distributors and traders.
click here to find a list of Fosinopril suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fosinopril CEP of the European Pharmacopoeia monograph is often referred to as a Fosinopril Certificate of Suitability (COS). The purpose of a Fosinopril CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Fosinopril EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Fosinopril to their clients by showing that a Fosinopril CEP has been issued for it. The manufacturer submits a Fosinopril CEP (COS) as part of the market authorization procedure, and it takes on the role of a Fosinopril CEP holder for the record. Additionally, the data presented in the Fosinopril CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Fosinopril DMF.
A Fosinopril CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Fosinopril 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 suppliers with CEP (COS) on PharmaCompass.
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