Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1M/s Aarti Pharmalabs ltd
02 1M/s Apitoria Pharma Limited
03 1M/s Lupin Limited
04 1M/s Solara Active Pharma Sciences Limited
01 1Quinapril Hydrochloride Ph. Eur
02 2Quinapril Hydrochloride USP
03 1Quinapril Hydrochloride USP/Ph. Eur
01 1WC-0017
02 1WC-0099
03 1WC-0127
04 1WC-0202n
01 4India
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Quinapril Hydrochloride USP/Ph. Eur
Date of Issue : 2022-08-24
Valid Till : 2025-07-29
Written Confirmation Number : WC-0099
Address of the Firm : Plot No.E-50, 50/1 and 59/1, Unit ?IV, MIDC, Tarapur?401506, Taluka: Palghar, Di...
Quinapril Hydrochloride Ph. Eur
Date of Issue : 2022-06-06
Valid Till : 2025-06-10
Written Confirmation Number : WC-0017
Address of the Firm : Unit-II, SurveyNo.:10&13,Gaddapotharam (Village), IDA-Kazipally, Jinnaram (Manda...
Date of Issue : 2022-07-23
Valid Till : 2025-07-04
Written Confirmation Number : WC-0202n
Address of the Firm : 198-202, New Industrial Area No.2, Mandideep-462046 Goharganj, Raisen-462046, Ma...
Date of Issue : 2022-08-31
Valid Till : 2025-08-04
Written Confirmation Number : WC-0127
Address of the Firm : A1/B, SIPCOT Industrial Complex, Kudikadu, Cuddalore -607005
47
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.
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A AC-1655 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AC-1655, including repackagers and relabelers. The FDA regulates AC-1655 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AC-1655 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 AC-1655 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AC-1655 supplier is an individual or a company that provides AC-1655 active pharmaceutical ingredient (API) or AC-1655 finished formulations upon request. The AC-1655 suppliers may include AC-1655 API manufacturers, exporters, distributors and traders.
click here to find a list of AC-1655 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A AC-1655 written confirmation (AC-1655 WC) is an official document issued by a regulatory agency to a AC-1655 manufacturer, verifying that the manufacturing facility of a AC-1655 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting AC-1655 APIs or AC-1655 finished pharmaceutical products to another nation, regulatory agencies frequently require a AC-1655 WC (written confirmation) as part of the regulatory process.
click here to find a list of AC-1655 suppliers with Written Confirmation (WC) on PharmaCompass.
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