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Lacosamide

NDC 69367-350 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerWestminster Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA205237
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLACOSAMIDE (150 mg/1)
Marketing started20230710
Package count1

External sources

Source: openFDA. Public-domain (CC0).