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lamotrigine

NDC 69117-0045 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namelamotrigine extended-release
Labeler / ManufacturerYiling Pharmaceutical, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213949
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsLAMOTRIGINE (50 mg/1)
Marketing started20211209
Package count3

External sources

Source: openFDA. Public-domain (CC0).