# Tretinoin

NDC: 59651-713
Generic name: Tretinoin
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GEL
Routes: TOPICAL
Marketing started: 20250227

FDA application: ANDA218245

## Active ingredients

- TRETINOIN: .25 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59651-713"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59651-713
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dea325b5-3cb8-4ffb-84e9-782f0e3f6b0e