# HYDROXYUREA

NDC: 0555-0882
Generic name: Hydroxyurea
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 19981019

FDA application: ANDA075143

## 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:"0555-0882"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0555-0882
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b9514ae5-79ae-4cc2-9d7f-c8f7806d1694