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Levetiracetam ER

NDC 69367-332 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic nameLevetiracetam
Labeler / ManufacturerWestminster Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA205130
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsLEVETIRACETAM (500 mg/1)
Marketing started20210930
Package count1

External sources

Source: openFDA. Public-domain (CC0).