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