FDA NDC Directory · JSON-LD · Markdown

Amantadine Hydrochloride

NDC 0591-4920 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208096
Dosage form / routeTABLET · ORAL
Active ingredientsAMANTADINE HYDROCHLORIDE (100 mg/1)
Marketing started20170103
Marketing ended20260630
Package count1

External sources

Source: openFDA. Public-domain (CC0).