# Lacosamide

NDC: 71921-221
Generic name: Lacosamide
Labeler / Manufacturer: Florida Pharmaceutical Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230921

FDA application: ANDA208308

## Active ingredients

- LACOSAMIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71921-221"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71921-221
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3680c0ff-7f5c-4572-b1eb-4fea96b7fbe2