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Lamotrigine

NDC 68382-984 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207763
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsLAMOTRIGINE (300 mg/1)
Marketing started20200514
Package count3

External sources

Source: openFDA. Public-domain (CC0).