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Levetiracetam

NDC 76494-528 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPrinston Pharmaceutical Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078106
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLEVETIRACETAM (250 mg/1)
Marketing started20120911
Package count1

External sources

Source: openFDA. Public-domain (CC0).