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Lamotrigine

NDC 46708-276 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA090607
Dosage form / routeTABLET · ORAL
Active ingredientsLAMOTRIGINE (150 mg/1)
Marketing started20130101
Package count5

External sources

Source: openFDA. Public-domain (CC0).