Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
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
01 1Quinapril Hydrochloride (Ph.Eur)
02 1Quinapril Hydrochloride (Ph.Eur./USP/IH)
03 1Quinapril Hydrochloride USP
04 1Quinapril Hydrochloride USP/EP
05 1Quinapril HydrochlorideJUSP)
01 1WC-0017
02 1WC-0099
03 1WC-0118
04 1WC-0127
05 1WC-0202
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 : 2019-07-05
Valid Till : 2022-07-04
Written Confirmation Number : WC-0202
Address of the Firm : 198-202, New Ind. Area No. 2, Mandideep- 462 046, Dist. Raisan (M.P), India.
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...
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 written confirmation (Quinapril hydrochloride WC) is an official document issued by a regulatory agency to a Quinapril hydrochloride manufacturer, verifying that the manufacturing facility of a Quinapril hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Quinapril hydrochloride APIs or Quinapril hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Quinapril hydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Quinapril hydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.
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