# Lacosamide

NDC: 47335-943
Generic name: Lacosamide
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220319

FDA application: ANDA205031

## Active ingredients

- LACOSAMIDE: 150 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-943"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-943
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2098d3a5-776e-4b52-8ade-80a3ab7b3de7