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Lamotrigine

NDC 62332-040 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090607
Dosage form / routeTABLET · ORAL
Active ingredientsLAMOTRIGINE (200 mg/1)
Marketing started20180205
Package count4

External sources

Source: openFDA. Public-domain (CC0).