# Tretinoin

NDC: 51672-1395
Generic name: tretinoin
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CREAM
Routes: TOPICAL
Marketing started: 20190122

FDA application: ANDA211645

## 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:"51672-1395"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-1395
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9e964be5-8d67-46a8-888e-0351f9113f68