01 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
02 1HETERO DRUGS LIMITED Hyderabad IN
03 1SIEGFRIED EVIONNAZ SA Evionnaz CH
04 2ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
01 4Fosinopril sodium
02 1Fosinopril sodium, Rhodium process
01 2China
02 2India
03 1Switzerland
01 5Valid
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
Fosinopril Sodium, Rhodium Process
Certificate Number : CEP 2024-433 - Rev 00
Status : Valid
Issue Date : 2025-01-29
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
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PharmaCompass offers a list of Fosinopril 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 Fosinopril manufacturer or Fosinopril supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fosinopril manufacturer or Fosinopril supplier.
PharmaCompass also assists you with knowing the Fosinopril API Price utilized in the formulation of products. Fosinopril API Price is not always fixed or binding as the Fosinopril Price is obtained through a variety of data sources. The Fosinopril Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fositens manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fositens, including repackagers and relabelers. The FDA regulates Fositens manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fositens 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 Fositens manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fositens supplier is an individual or a company that provides Fositens active pharmaceutical ingredient (API) or Fositens finished formulations upon request. The Fositens suppliers may include Fositens API manufacturers, exporters, distributors and traders.
click here to find a list of Fositens suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fositens CEP of the European Pharmacopoeia monograph is often referred to as a Fositens Certificate of Suitability (COS). The purpose of a Fositens CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Fositens EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Fositens to their clients by showing that a Fositens CEP has been issued for it. The manufacturer submits a Fositens CEP (COS) as part of the market authorization procedure, and it takes on the role of a Fositens CEP holder for the record. Additionally, the data presented in the Fositens CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Fositens DMF.
A Fositens CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Fositens 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 Fositens suppliers with CEP (COS) on PharmaCompass.
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