Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1AARTI INDUSTRIES LIMITED Mulund (W), Mumbai IN
02 1AARTI PHARMALABS LIMITED Mulund (W), Mumbai IN
03 1Farmhispania, S.A. Montmeló ES
04 1UNIMARK REMEDIES LIMITED Mumbai IN
05 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
06 1SCINOPHARM TAIWAN, LTD. Shan-Hua TW
07 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
08 1Wisdom Pharmaceutical Co., Ltd. Haimen CN
09 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Benazepril Hydrochloride, Process 2
Certificate Number : R0-CEP 2023-055 - Rev 00
Status : Valid
Issue Date : 2023-07-07
Type : Chemical
Substance Number : 2388
Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
Certificate Number : R1-CEP 2009-261 - Rev 00
Status : Valid
Issue Date : 2016-01-26
Type : Chemical
Substance Number : 2388
Certificate Number : R1-CEP 2008-273 - Rev 00
Status : Suspended by Holder
Issue Date : 2015-04-15
Type : Chemical
Substance Number : 2388
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Certificate Number : R1-CEP 2011-197 - Rev 00
Status : Valid
Issue Date : 2018-05-16
Type : Chemical
Substance Number : 2388
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PharmaCompass offers a list of Benazepril Hydrochloride 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 Benazepril Hydrochloride manufacturer or Benazepril Hydrochloride supplier for your needs.
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A Zinadril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zinadril, including repackagers and relabelers. The FDA regulates Zinadril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zinadril API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Zinadril supplier is an individual or a company that provides Zinadril active pharmaceutical ingredient (API) or Zinadril finished formulations upon request. The Zinadril suppliers may include Zinadril API manufacturers, exporters, distributors and traders.
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A Zinadril CEP of the European Pharmacopoeia monograph is often referred to as a Zinadril Certificate of Suitability (COS). The purpose of a Zinadril CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Zinadril EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Zinadril to their clients by showing that a Zinadril CEP has been issued for it. The manufacturer submits a Zinadril CEP (COS) as part of the market authorization procedure, and it takes on the role of a Zinadril CEP holder for the record. Additionally, the data presented in the Zinadril CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Zinadril DMF.
A Zinadril CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Zinadril CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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