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Amantadine Hydrochloride

NDC 0832-0111 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameamantadine hydrochloride
Labeler / ManufacturerUpsher-Smith Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076186
Dosage form / routeTABLET · ORAL
Active ingredientsAMANTADINE HYDROCHLORIDE (100 mg/1)
Marketing started20111215
Marketing ended20280229
Package count3

External sources

Source: openFDA. Public-domain (CC0).