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