# Zyrtec

NDC: 50580-753
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Kenvue Brands LLC
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, CHEWABLE
Routes: ORAL
Marketing started: 20220620

FDA application: NDA021621

## 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:"50580-753"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50580-753
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dc613bd5-70fd-1d9b-e053-2995a90a41cd