# Isotretinoin

NDC: 68308-571
Generic name: Isotretinoin
Labeler / Manufacturer: Mayne Pharma
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20210921

FDA application: ANDA212333

## Active ingredients

- ISOTRETINOIN: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68308-571"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68308-571
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ebe1b3e3-1013-4cf6-bdc8-2baa3dc26e16