Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1AARTI PHARMALABS LIMITED Mulund (W), Mumbai IN
02 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
03 1MYLAN LABORATORIES LIMITED Hyderabad IN
04 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
01 4Quinapril hydrochloride
01 1China
02 2India
03 1U.S.A
01 3Valid
02 1Withdrawn by Holder
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Certificate Number : R1-CEP 2016-100 - Rev 00
Status : Valid
Issue Date : 2023-02-01
Type : Chemical
Substance Number : 1763
Certificate Number : CEP 2013-160 - Rev 02
Status : Valid
Issue Date : 2023-11-16
Type : Chemical
Substance Number : 1763
Certificate Number : R0-CEP 2012-411 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2017-09-18
Type : Chemical
Substance Number : 1763
Certificate Number : R1-CEP 2013-102 - Rev 02
Status : Valid
Issue Date : 2020-09-16
Type : Chemical
Substance Number : 1763
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PharmaCompass offers a list of Quinapril 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 Quinapril manufacturer or Quinapril supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Quinapril manufacturer or Quinapril supplier.
PharmaCompass also assists you with knowing the Quinapril API Price utilized in the formulation of products. Quinapril API Price is not always fixed or binding as the Quinapril Price is obtained through a variety of data sources. The Quinapril Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ectren manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ectren, including repackagers and relabelers. The FDA regulates Ectren manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ectren 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 Ectren manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ectren supplier is an individual or a company that provides Ectren active pharmaceutical ingredient (API) or Ectren finished formulations upon request. The Ectren suppliers may include Ectren API manufacturers, exporters, distributors and traders.
click here to find a list of Ectren suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ectren CEP of the European Pharmacopoeia monograph is often referred to as a Ectren Certificate of Suitability (COS). The purpose of a Ectren CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ectren EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ectren to their clients by showing that a Ectren CEP has been issued for it. The manufacturer submits a Ectren CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ectren CEP holder for the record. Additionally, the data presented in the Ectren CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ectren DMF.
A Ectren CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ectren 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 Ectren suppliers with CEP (COS) on PharmaCompass.
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