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Amantadine Hydrochloride

NDC 10135-692 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMarlex Pharmaceuticals Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA210215
Dosage form / routeTABLET · ORAL
Active ingredientsAMANTADINE HYDROCHLORIDE (100 mg/1)
Marketing started20200301
Package count2

External sources

Source: openFDA. Public-domain (CC0).