Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
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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
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01 8Benazepril hydrochloride
02 1Benazepril hydrochloride, Process 2
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01 2China
02 5India
03 1Spain
04 1Taiwan
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01 1Suspended by Holder
02 8Valid
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.
Benazepril Hydrochloride, Process 2
Certificate Number : R0-CEP 2023-055 - Rev 00
Status : Valid
Issue Date : 2023-07-07
Type : Chemical
Substance Number : 2388
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.
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
Certificate Number : CEP 2008-232 - Rev 03
Status : Valid
Issue Date : 2023-11-16
Type : Chemical
Substance Number : 2388
Certificate Number : CEP 2009-356 - Rev 03
Status : Valid
Issue Date : 2024-09-11
Type : Chemical
Substance Number : 2388
Certificate Number : R1-CEP 2009-220 - Rev 01
Status : Valid
Issue Date : 2016-08-26
Type : Chemical
Substance Number : 2388
Certificate Number : R1-CEP 2015-322 - Rev 00
Status : Valid
Issue Date : 2023-01-11
Type : Chemical
Substance Number : 2388
Certificate Number : R1-CEP 2010-276 - Rev 00
Status : Valid
Issue Date : 2017-06-02
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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PharmaCompass also assists you with knowing the Benazepril Hydrochloride API Price utilized in the formulation of products. Benazepril Hydrochloride API Price is not always fixed or binding as the Benazepril Hydrochloride Price is obtained through a variety of data sources. The Benazepril Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A KB-65121 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KB-65121, including repackagers and relabelers. The FDA regulates KB-65121 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KB-65121 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 KB-65121 supplier is an individual or a company that provides KB-65121 active pharmaceutical ingredient (API) or KB-65121 finished formulations upon request. The KB-65121 suppliers may include KB-65121 API manufacturers, exporters, distributors and traders.
click here to find a list of KB-65121 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A KB-65121 CEP of the European Pharmacopoeia monograph is often referred to as a KB-65121 Certificate of Suitability (COS). The purpose of a KB-65121 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of KB-65121 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of KB-65121 to their clients by showing that a KB-65121 CEP has been issued for it. The manufacturer submits a KB-65121 CEP (COS) as part of the market authorization procedure, and it takes on the role of a KB-65121 CEP holder for the record. Additionally, the data presented in the KB-65121 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the KB-65121 DMF.
A KB-65121 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. KB-65121 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 KB-65121 suppliers with CEP (COS) on PharmaCompass.
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