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Lamotrigine

NDC 0228-1638 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA200672
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsLAMOTRIGINE (250 mg/1)
Marketing started20160601
Package count1

External sources

Source: openFDA. Public-domain (CC0).