# TRETINOIN

NDC: 21922-042
Generic name: Tretinoin
Labeler / Manufacturer: Encube Ethicals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GEL
Routes: TOPICAL
Marketing started: 20260416

FDA application: ANDA215609

## Active ingredients

- TRETINOIN: .6 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"21922-042"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=21922-042
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=57558405-42fa-40bb-a61c-48e030d976de