Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
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01 1M/s. Aarti Pharmalabs Limited
02 1M/s. Aurobindo Pharma Ltd.,
03 1M/s. Lupin Ltd
04 1M/s. Mylan Laboratories Ltd.,
05 1Solara Active Pharma Sciences Limited
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01 1Quinapril Hydrochloride (Ph.Eur)
02 1Quinapril Hydrochloride (Ph.Eur./USP/IH)
03 1Quinapril Hydrochloride (USP)
04 1Quinapril Hydrochloride USP
05 1Quinapril Hydrochloride USP/EP
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01 1WC-0017
02 1WC-0099
03 1WC-0118
04 1WC-0127
05 1WC-0202
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01 5India
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Quinapril Hydrochloride USP/EP
Date of Issue : 2023-01-06
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: Pal...
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 No. VIII, Sy. No. 10 & 13, Gaddapotharam Village, I,D.A. Kazipally, Jinnara...
Date of Issue : 2022-07-13
Valid Till : 2025-07-04
Written Confirmation Number : WC-0202
Address of the Firm : 198-202, New Industrial Area No.2, Mandideep - 462046 Goharganj, Raisen-462046, ...
Date of Issue : 2022-09-30
Valid Till : 2025-08-04
Written Confirmation Number : WC-0127
Address of the Firm : A1/B, SIPCOT Industrial Complex, Kudikadu, Cuddalore-607 005
Quinapril Hydrochloride (Ph.Eur./USP/IH)
Date of Issue : 2019-08-05
Valid Till : 2022-08-04
Written Confirmation Number : WC-0118
Address of the Firm : Unit -1, Sy No.10, Gaddapotharam (V), Khazipally Industrial Area,Medak Dist.,A.P...
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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.
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A Accuprin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Accuprin, including repackagers and relabelers. The FDA regulates Accuprin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Accuprin 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 Accuprin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Accuprin supplier is an individual or a company that provides Accuprin active pharmaceutical ingredient (API) or Accuprin finished formulations upon request. The Accuprin suppliers may include Accuprin API manufacturers, exporters, distributors and traders.
click here to find a list of Accuprin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Accuprin written confirmation (Accuprin WC) is an official document issued by a regulatory agency to a Accuprin manufacturer, verifying that the manufacturing facility of a Accuprin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Accuprin APIs or Accuprin finished pharmaceutical products to another nation, regulatory agencies frequently require a Accuprin WC (written confirmation) as part of the regulatory process.
click here to find a list of Accuprin suppliers with Written Confirmation (WC) on PharmaCompass.
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