01 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
02 1HETERO DRUGS LIMITED Hyderabad IN
03 2ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
01 3Fosinopril sodium
02 1Fosinopril sodium, Rhodium process
01 2China
02 2India
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 03
Status : Valid
Issue Date : 2025-11-12
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 Sodium, Fosinopril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium, Fosinopril, including repackagers and relabelers. The FDA regulates Sodium, Fosinopril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium, 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 Sodium, Fosinopril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium, Fosinopril supplier is an individual or a company that provides Sodium, Fosinopril active pharmaceutical ingredient (API) or Sodium, Fosinopril finished formulations upon request. The Sodium, Fosinopril suppliers may include Sodium, Fosinopril API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium, Fosinopril suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sodium, Fosinopril CEP of the European Pharmacopoeia monograph is often referred to as a Sodium, Fosinopril Certificate of Suitability (COS). The purpose of a Sodium, Fosinopril CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Sodium, Fosinopril EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Sodium, Fosinopril to their clients by showing that a Sodium, Fosinopril CEP has been issued for it. The manufacturer submits a Sodium, Fosinopril CEP (COS) as part of the market authorization procedure, and it takes on the role of a Sodium, Fosinopril CEP holder for the record. Additionally, the data presented in the Sodium, Fosinopril CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Sodium, Fosinopril DMF.
A Sodium, Fosinopril CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Sodium, 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 Sodium, Fosinopril suppliers with CEP (COS) on PharmaCompass.
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