Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
01 1Farmhispania, S.A. Montmeló ES
02 1Wockhardt Limited Mumbai IN
03 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
04 1ZHONGFU PHARMACEUTICAL CO., LTD. Weifang City CN
01 4Captopril
01 2China
02 1India
03 1Spain
01 4Valid
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 1997-023 - 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
77
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Captopril manufacturer or Captopril supplier.
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 Acepress manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acepress, including repackagers and relabelers. The FDA regulates Acepress manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acepress 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 Acepress manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Acepress supplier is an individual or a company that provides Acepress active pharmaceutical ingredient (API) or Acepress finished formulations upon request. The Acepress suppliers may include Acepress API manufacturers, exporters, distributors and traders.
click here to find a list of Acepress suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Acepress CEP of the European Pharmacopoeia monograph is often referred to as a Acepress Certificate of Suitability (COS). The purpose of a Acepress CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Acepress EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Acepress to their clients by showing that a Acepress CEP has been issued for it. The manufacturer submits a Acepress CEP (COS) as part of the market authorization procedure, and it takes on the role of a Acepress CEP holder for the record. Additionally, the data presented in the Acepress CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Acepress DMF.
A Acepress CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Acepress 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 Acepress suppliers with CEP (COS) on PharmaCompass.
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