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