Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
01 1Farmhispania, S.A. Montmeló ES
02 1EGIS Pharmaceuticals PLC Budapest HU
03 1Wockhardt Limited Mumbai IN
04 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
05 1ZHONGFU PHARMACEUTICAL CO., LTD. Weifang City CN
01 5Captopril
01 2China
02 1Hungary
03 1India
04 1Spain
01 4Valid
02 1Withdrawn by Holder
Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
Certificate Number : R1-CEP 1997-018 - Rev 06
Status : Valid
Issue Date : 2011-03-01
Type : Chemical
Substance Number : 1079
Certificate Number : R1-CEP 1998-052 - Rev 04
Status : Valid
Issue Date : 2014-06-24
Type : Chemical
Substance Number : 1079
Certificate Number : R1-CEP 1997-101 - Rev 04
Status : Withdrawn by Holder
Issue Date : 2011-12-19
Type : Chemical
Substance Number : 1079
Certificate Number : R1-CEP 1997-023 - Rev 10
Status : Valid
Issue Date : 2020-10-19
Type : Chemical
Substance Number : 1079
Certificate Number : R1-CEP 2003-113 - Rev 02
Status : Valid
Issue Date : 2016-10-07
Type : Chemical
Substance Number : 1079
A Captopril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Captopril, including repackagers and relabelers. The FDA regulates Captopril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Captopril 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 Captopril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Captopril supplier is an individual or a company that provides Captopril active pharmaceutical ingredient (API) or Captopril finished formulations upon request. The Captopril suppliers may include Captopril API manufacturers, exporters, distributors and traders.
click here to find a list of Captopril suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Captopril CEP of the European Pharmacopoeia monograph is often referred to as a Captopril Certificate of Suitability (COS). The purpose of a Captopril CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Captopril EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Captopril to their clients by showing that a Captopril CEP has been issued for it. The manufacturer submits a Captopril CEP (COS) as part of the market authorization procedure, and it takes on the role of a Captopril CEP holder for the record. Additionally, the data presented in the Captopril CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Captopril DMF.
A Captopril CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Captopril 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 Captopril suppliers with CEP (COS) on PharmaCompass.
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