# Isotretinoin

NDC: 70771-1666
Generic name: Isotretinoin
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20250609

FDA application: ANDA216633

## Active ingredients

- ISOTRETINOIN: 35 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70771-1666"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70771-1666
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=245898e5-3a61-4d6a-8375-8b3a8b7364ac