FDA NDC Directory · JSON-LD · Markdown

Lacosamide

NDC 29300-366 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerUnichem Pharmaceuticals (USA), Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213109
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLACOSAMIDE (150 mg/1)
Marketing started20241201
Package count2

External sources

Source: openFDA. Public-domain (CC0).