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Status : Withdrawn by Holder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
88
PharmaCompass offers a list of Captopril 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 Captopril manufacturer or Captopril supplier for your needs.
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PharmaCompass also assists you with knowing the Captopril API Price utilized in the formulation of products. Captopril API Price is not always fixed or binding as the Captopril Price is obtained through a variety of data sources. The Captopril Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lopril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lopril, including repackagers and relabelers. The FDA regulates Lopril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lopril 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 Lopril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lopril supplier is an individual or a company that provides Lopril active pharmaceutical ingredient (API) or Lopril finished formulations upon request. The Lopril suppliers may include Lopril API manufacturers, exporters, distributors and traders.
click here to find a list of Lopril suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lopril CEP of the European Pharmacopoeia monograph is often referred to as a Lopril Certificate of Suitability (COS). The purpose of a Lopril CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Lopril EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Lopril to their clients by showing that a Lopril CEP has been issued for it. The manufacturer submits a Lopril CEP (COS) as part of the market authorization procedure, and it takes on the role of a Lopril CEP holder for the record. Additionally, the data presented in the Lopril CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Lopril DMF.
A Lopril CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Lopril 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 Lopril suppliers with CEP (COS) on PharmaCompass.
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