# Tretinoin

NDC: 69238-2323
Generic name: Tretinoin
Labeler / Manufacturer: Amneal Pharmaceuticals NY LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GEL
Routes: TOPICAL
Marketing started: 20260515

FDA application: ANDA217497

## 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:"69238-2323"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69238-2323
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4b6006e3-f7a4-4823-8217-3e5b0f7e58d9