A Ibogamine, 12-methoxy-, monohydrochloride (9CI) DMF (Drug Master File) is a document detailing the whole manufacturing process of Ibogamine, 12-methoxy-, monohydrochloride (9CI) active pharmaceutical ingredient (API) in detail. Different forms of Ibogamine, 12-methoxy-, monohydrochloride (9CI) DMFs exist exist since differing nations have different regulations, such as Ibogamine, 12-methoxy-, monohydrochloride (9CI) USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ibogamine, 12-methoxy-, monohydrochloride (9CI) DMF submitted to regulatory agencies in the US is known as a USDMF. Ibogamine, 12-methoxy-, monohydrochloride (9CI) USDMF includes data on Ibogamine, 12-methoxy-, monohydrochloride (9CI)'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ibogamine, 12-methoxy-, monohydrochloride (9CI) USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ibogamine, 12-methoxy-, monohydrochloride (9CI) suppliers with USDMF on PharmaCompass.