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Lamotrigine

NDC 55111-428 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerDr.Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202383
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsLAMOTRIGINE (300 mg/1)
Marketing started20130620
Package count3

External sources

Source: openFDA. Public-domain (CC0).