# Isotretinoin

NDC: 0832-8301
Generic name: Isotretinoin
Labeler / Manufacturer: Upsher-Smith Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20120501

FDA application: ANDA076485

## Active ingredients

- ISOTRETINOIN: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0832-8301"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0832-8301
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c369e1c3-90c5-4768-9741-56c62253a2c4