# Cetirizine

NDC: 55154-8081
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Cardinal Health 107, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20180629
Marketing ended: 20260630
FDA application: ANDA078336

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55154-8081"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55154-8081
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6f3c2e57-7a0f-432f-a7f1-04906f5e4ddf