# Tretinoin

NDC: 46708-809
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: 20250816

FDA application: ANDA218399

## Active ingredients

- TRETINOIN: .25 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"46708-809"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46708-809
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4e96fb71-14f4-4789-91af-ba94b0879162