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Lacosamide

NDC 33342-302 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA208466
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLACOSAMIDE (50 mg/1)
Marketing started20240524
Package count2

External sources

Source: openFDA. Public-domain (CC0).