# HYDROXYUREA

NDC: 70069-820
Generic name: HYDROXYUREA
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20240618

FDA application: ANDA218021

## Active ingredients

- HYDROXYUREA: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-820"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-820
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9752a347-b42c-44d5-8fd1-c538f7f239dc