# HYDROXYUREA

NDC: 67184-0607
Generic name: HYDROXYUREA
Labeler / Manufacturer: Qilu Pharmaceutical Co., Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20240306

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:"67184-0607"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67184-0607
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4cd244d4-bd4a-41c8-b072-c2135787d412