01 1Mitsubishi Corporation
01 1ALTHIAZIDE
01 1Japan
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 845
Submission : 1964-09-30
Status : Inactive
Type : II
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A Althiazide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Althiazide, including repackagers and relabelers. The FDA regulates Althiazide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Althiazide 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 Althiazide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Althiazide supplier is an individual or a company that provides Althiazide active pharmaceutical ingredient (API) or Althiazide finished formulations upon request. The Althiazide suppliers may include Althiazide API manufacturers, exporters, distributors and traders.
click here to find a list of Althiazide suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Althiazide DMF (Drug Master File) is a document detailing the whole manufacturing process of Althiazide active pharmaceutical ingredient (API) in detail. Different forms of Althiazide DMFs exist exist since differing nations have different regulations, such as Althiazide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Althiazide DMF submitted to regulatory agencies in the US is known as a USDMF. Althiazide USDMF includes data on Althiazide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Althiazide USDMF is kept confidential to protect the manufacturer’s intellectual property.
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