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Lamotrigine

NDC 46708-417 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA211821
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsLAMOTRIGINE (200 mg/1)
Marketing started20241007
Package count2

External sources

Source: openFDA. Public-domain (CC0).