FDA NDC Directory · JSON-LD · Markdown

Galantamine

NDC 57237-049 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090957
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsGALANTAMINE HYDROBROMIDE (4 mg/1)
Marketing started20110329
Package count1

External sources

Source: openFDA. Public-domain (CC0).