Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1Aarti Pharmalabs
02 1Farmhispania
03 1Aurobindo Pharma Limited
04 1Esteve Quimica
05 1Lupin Ltd
06 1RANBAXY LABORATORIES LIMITED
07 1Signa S.A. de C.V.
08 1Solara Active Pharma Sciences
09 1Sun Pharmaceutical Industries Limited
10 1Viatris
11 1Zhejiang Huahai Pharmaceutical
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
GDUFA
DMF Review : Complete
Rev. Date : 2021-01-07
Pay. Date : 2020-12-31
DMF Number : 19413
Submission : 2006-05-08
Status :
Type : II
Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16735
Submission : 2003-07-25
Status :
Type : II
A Quinapril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Quinapril, including repackagers and relabelers. The FDA regulates Quinapril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Quinapril 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 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Quinapril supplier is an individual or a company that provides Quinapril active pharmaceutical ingredient (API) or Quinapril finished formulations upon request. The Quinapril suppliers may include Quinapril API manufacturers, exporters, distributors and traders.
click here to find a list of Quinapril suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Quinapril DMF (Drug Master File) is a document detailing the whole manufacturing process of Quinapril active pharmaceutical ingredient (API) in detail. Different forms of Quinapril DMFs exist exist since differing nations have different regulations, such as Quinapril USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Quinapril DMF submitted to regulatory agencies in the US is known as a USDMF. Quinapril USDMF includes data on Quinapril's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Quinapril USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Quinapril suppliers with USDMF on PharmaCompass.
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