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
A Verapamil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Verapamil, including repackagers and relabelers. The FDA regulates Verapamil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Verapamil 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 Verapamil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Verapamil supplier is an individual or a company that provides Verapamil active pharmaceutical ingredient (API) or Verapamil finished formulations upon request. The Verapamil suppliers may include Verapamil API manufacturers, exporters, distributors and traders.
click here to find a list of Verapamil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Verapamil DMF (Drug Master File) is a document detailing the whole manufacturing process of Verapamil active pharmaceutical ingredient (API) in detail. Different forms of Verapamil DMFs exist exist since differing nations have different regulations, such as Verapamil USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Verapamil DMF submitted to regulatory agencies in the US is known as a USDMF. Verapamil USDMF includes data on Verapamil's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Verapamil USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Verapamil suppliers with USDMF on PharmaCompass.
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