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Levetiracetam

NDC 50228-472 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerScieGen Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA215069
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLEVETIRACETAM (750 mg/1)
Marketing started20210611
Package count3

External sources

Source: openFDA. Public-domain (CC0).