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