# Acitretin

NDC: 0115-1752
Generic name: Acitretin
Labeler / Manufacturer: Amneal Pharmaceuticals of New York LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20160104

FDA application: ANDA202552

## Active ingredients

- ACITRETIN: 22.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0115-1752"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0115-1752
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=85507f6c-f802-479e-bacc-624b5136d092