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Galantamine

NDC 70436-005 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namegalantamine
Labeler / ManufacturerSlate Run Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077604
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsGALANTAMINE HYDROBROMIDE (8 mg/1)
Marketing started20170802
Package count1

External sources

Source: openFDA. Public-domain (CC0).