# Tretinoin

NDC: 46708-807
Generic name: Tretinoin
Labeler / Manufacturer: Alembic Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CREAM
Routes: TOPICAL
Marketing started: 20250425

FDA application: ANDA217804

## 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:"46708-807"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46708-807
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7845d60d-7c4c-4854-a417-6d3ea86a710f