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Lamotrigine Extended Release

NDC 49884-604 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namelamotrigine extended release
Labeler / ManufacturerPar Health USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA201791
Dosage form / routeTABLET · ORAL
Active ingredientsLAMOTRIGINE (250 mg/1)
Marketing started20130118
Marketing ended20260930
Package count1

External sources

Source: openFDA. Public-domain (CC0).