A Citric acid, anhydrous (USP) DMF (Drug Master File) is a document detailing the whole manufacturing process of Citric acid, anhydrous (USP) active pharmaceutical ingredient (API) in detail. Different forms of Citric acid, anhydrous (USP) DMFs exist exist since differing nations have different regulations, such as Citric acid, anhydrous (USP) USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Citric acid, anhydrous (USP) DMF submitted to regulatory agencies in the US is known as a USDMF. Citric acid, anhydrous (USP) USDMF includes data on Citric acid, anhydrous (USP)'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Citric acid, anhydrous (USP) USDMF is kept confidential to protect the manufacturer’s intellectual property.
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