# Tretinoin

NDC: 10370-268
Generic name: Tretinoin
Labeler / Manufacturer: Par Health USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20121024

FDA application: ANDA201687

## Active ingredients

- TRETINOIN: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"10370-268"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10370-268
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c4ae9d9-c2a0-4995-a27a-e3f0f0284db9