# Tretinoin

NDC: 0378-8090
Generic name: Tretinoin
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GEL
Routes: TOPICAL
Marketing started: 20181114

FDA application: ANDA207955

## Active ingredients

- TRETINOIN: .5 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-8090"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-8090
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ce5f4f14-5e60-4cc1-bcb3-1fa9b8aa9cd5