# Cetirizine Hydrochloride

NDC: 85293-001
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Umasuto, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250304

FDA application: ANDA077829

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"85293-001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=85293-001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9af4ab23-d6d3-43f9-a026-76fd9771963f