# Tretinoin

NDC: 72162-2303
Generic name: Tretinoin
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GEL
Routes: TOPICAL
Marketing started: 20230824

FDA application: ANDA215609

## Active ingredients

- TRETINOIN: .8 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72162-2303"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-2303
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2b58cf56-e713-4cdd-8b4e-e6651ef76650