# Tretinoin

NDC: 68071-3826
Generic name: tretinoin
Labeler / Manufacturer: NuCare Pharmaceuticals, 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:"68071-3826"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-3826
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=31d2cd00-e534-6755-e063-6394a90ab8bb