# Tretinoin

NDC: 21922-079
Generic name: Tretinoin
Labeler / Manufacturer: Encube Ethicals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CREAM
Routes: TOPICAL
Marketing started: 20250711

FDA application: ANDA217831

## 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:"21922-079"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=21922-079
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5e3fb8ea-234c-4be2-95a7-d139e069cf98