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Lamotrigine

NDC 65841-686 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA077633
Dosage form / routeTABLET · ORAL
Active ingredientsLAMOTRIGINE (200 mg/1)
Marketing started20090127
Package count3

External sources

Source: openFDA. Public-domain (CC0).