# Zyrtec Allergy

NDC: 67751-192
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Navajo Manufacturing Company Incorporated
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20191120

FDA application: NDA019835

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67751-192"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67751-192
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c4693cb-f066-0666-e053-2a95a90a96d3