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Amantadine Hydrochloride

NDC 60760-779 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerST. MARY'S MEDICAL PARK PHARMACY
Marketing categoryAbbreviated NDA (generic) · App ANDA212044
Dosage form / routeCAPSULE · ORAL
Active ingredientsAMANTADINE HYDROCHLORIDE (100 mg/1)
Marketing started20200521
Package count1

External sources

Source: openFDA. Public-domain (CC0).