# Ursodiol

NDC: 70710-1127
Generic name: Ursodiol
Labeler / Manufacturer: Zydus Pharmaceuticals (USA) Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20181107

FDA application: ANDA211145

## Active ingredients

- URSODIOL: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70710-1127"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1127
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=55c1556b-8b47-479a-979b-fd61bdd27c7f