01 1Abbott Laboratories
01 1VERAPAMIL AS MNFG IN N.CHICAGO, ILLINOIS
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4910
Submission : 1983-03-31
Status : Inactive
Type : II
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A Tarka manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tarka, including repackagers and relabelers. The FDA regulates Tarka manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tarka 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 Tarka manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Tarka supplier is an individual or a company that provides Tarka active pharmaceutical ingredient (API) or Tarka finished formulations upon request. The Tarka suppliers may include Tarka API manufacturers, exporters, distributors and traders.
click here to find a list of Tarka suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Tarka DMF (Drug Master File) is a document detailing the whole manufacturing process of Tarka active pharmaceutical ingredient (API) in detail. Different forms of Tarka DMFs exist exist since differing nations have different regulations, such as Tarka USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tarka DMF submitted to regulatory agencies in the US is known as a USDMF. Tarka USDMF includes data on Tarka's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tarka USDMF is kept confidential to protect the manufacturer’s intellectual property.
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