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Levetiracetam

NDC 60505-3517 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA091261
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsLEVETIRACETAM (750 mg/1)
Marketing started20110912
Package count2

External sources

Source: openFDA. Public-domain (CC0).