# Felbamate

NDC: 62559-731
Generic name: Felbamate
Labeler / Manufacturer: ANI Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180904

FDA application: ANDA202284

## Active ingredients

- FELBAMATE: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62559-731"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62559-731
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=17850520-f823-4d05-8f9b-5eadfa68bae2