# Adapalene and Benzoyl Peroxide

NDC: 51672-1384
Generic name: ADAPALENE and BENZOYL PEROXIDE
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GEL
Routes: TOPICAL
Marketing started: 20181017

FDA application: ANDA209148

## Active ingredients

- ADAPALENE: 3 mg/g
- BENZOYL PEROXIDE: 25 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-1384"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-1384
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=13fc72e9-7178-4a8b-9fe8-d88ba591dac8