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Galantamine

NDC 72162-2566 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA090957
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsGALANTAMINE HYDROBROMIDE (8 mg/1)
Marketing started20110329
Package count1

External sources

Source: openFDA. Public-domain (CC0).