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Lamotrigine

NDC 65162-956 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207497
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsLAMOTRIGINE (50 mg/1)
Marketing started20181130
Package count2

External sources

Source: openFDA. Public-domain (CC0).