# Tretinoin

NDC: 68084-075
Generic name: Tretinoin
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20130718

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:"68084-075"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68084-075
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b22d5a07-623a-4645-b87d-a151b86da8d5