# PERAMPANEL

NDC: 51672-4256
Generic name: PERAMPANEL
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20260616

FDA application: ANDA219052

## Active ingredients

- PERAMPANEL: .5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-4256"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-4256
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3c72a5f7-bb22-4c48-942a-543ca84ed5a9