# Cetirizine hydrochloride

NDC: 80513-731
Generic name: Cetirizine hydrochloride
Labeler / Manufacturer: Advanced Rx LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20250501

FDA application: ANDA209274

## 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:"80513-731"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80513-731
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=737492bf-96bd-4f7c-aa42-4910746f44bb