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
01 1QUINAPRIL HCL
02 2QUINAPRIL HYDROCHLORIDE
03 1QUINAPRIL HYDROCHLORIDE ACETONE SOLVATE
04 7QUINAPRIL HYDROCHLORIDE USP
01 1China
02 6India
03 1Mexico
04 2Spain
05 1U.S.A
01 5Active
02 6Inactive
01 2Complete
02 9Blank
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 : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16735
Submission : 2003-07-25
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19046
Submission : 2005-11-30
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12471
Submission : 1997-04-14
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17957
Submission : 2004-12-31
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16261
Submission : 2002-11-27
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15619
Submission : 2001-09-14
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20333
Submission : 2007-03-08
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21476
Submission : 2008-03-22
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-07-23
Pay. Date : 2012-11-23
DMF Number : 20315
Submission : 2006-10-17
Status : Active
Type : II
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 DMF (Drug Master File) is a document detailing the whole manufacturing process of Quinapril hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Quinapril hydrochloride DMFs exist exist since differing nations have different regulations, such as Quinapril hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Quinapril hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Quinapril hydrochloride USDMF includes data on Quinapril hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Quinapril hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Quinapril hydrochloride suppliers with USDMF on PharmaCompass.
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