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LAMICTAL XR

NDC 0173-0761 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namelamotrigine
Labeler / ManufacturerGlaxoSmithKline LLC
Marketing categoryNew Drug Application (innovator) · App NDA022115
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsLAMOTRIGINE (300 mg/1)
Marketing started20110331
Package count1

External sources

Source: openFDA. Public-domain (CC0).