# Tretinoin

NDC: 59651-712
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: 20250113

FDA application: ANDA218246

## Active ingredients

- TRETINOIN: .1 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59651-712"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59651-712
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f64e45d7-bbc0-4da4-9ccb-e3941f22fdbe