FDA NDC Directory · JSON-LD · Markdown

Amantadine Hydrochloride

NDC 42543-497 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerStrides Pharma Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209035
Dosage form / routeTABLET · ORAL
Active ingredientsAMANTADINE HYDROCHLORIDE (100 mg/1)
Marketing started20170804
Package count2

External sources

Source: openFDA. Public-domain (CC0).