A Rhodamine 123 DMF (Drug Master File) is a document detailing the whole manufacturing process of Rhodamine 123 active pharmaceutical ingredient (API) in detail. Different forms of Rhodamine 123 DMFs exist exist since differing nations have different regulations, such as Rhodamine 123 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Rhodamine 123 DMF submitted to regulatory agencies in the US is known as a USDMF. Rhodamine 123 USDMF includes data on Rhodamine 123's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Rhodamine 123 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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