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LEVETIRACETAM

NDC 42658-149 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerHisun Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207175
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsLEVETIRACETAM (750 mg/1)
Marketing started20250101
Package count2

External sources

Source: openFDA. Public-domain (CC0).