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Lamotrigine Extended-Release

NDC 10370-334 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namelamotrigine
Labeler / ManufacturerPar Health USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA201374
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsLAMOTRIGINE (250 mg/1)
Marketing started20260102
Package count1

External sources

Source: openFDA. Public-domain (CC0).