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Status : Withdrawn by Holder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
A Quinapril hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Quinapril hydrochloride, including repackagers and relabelers. The FDA regulates Quinapril hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Quinapril hydrochloride 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 Quinapril hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Quinapril hydrochloride supplier is an individual or a company that provides Quinapril hydrochloride active pharmaceutical ingredient (API) or Quinapril hydrochloride finished formulations upon request. The Quinapril hydrochloride suppliers may include Quinapril hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Quinapril hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Quinapril hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Quinapril hydrochloride Certificate of Suitability (COS). The purpose of a Quinapril hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Quinapril hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Quinapril hydrochloride to their clients by showing that a Quinapril hydrochloride CEP has been issued for it. The manufacturer submits a Quinapril hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Quinapril hydrochloride CEP holder for the record. Additionally, the data presented in the Quinapril hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Quinapril hydrochloride DMF.
A Quinapril hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Quinapril hydrochloride 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 Quinapril hydrochloride suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering Quinapril hydrochloride
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