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Lamotrigine

NDC 16571-786 · HUMAN PRESCRIPTION DRUG · TABLET, CHEWABLE

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090401
Dosage form / routeTABLET, CHEWABLE · ORAL
Active ingredientsLAMOTRIGINE (25 mg/1)
Marketing started20091104
Package count1

External sources

Source: openFDA. Public-domain (CC0).