FDA NDC Directory · JSON-LD · Markdown

Amantadine

NDC 67046-1531 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCoupler LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA214284
Dosage form / routeTABLET · ORAL
Active ingredientsAMANTADINE HYDROCHLORIDE (100 mg/1)
Marketing started20250313
Package count1

External sources

Source: openFDA. Public-domain (CC0).