# ZYRTEC-D

NDC: 50580-719
Generic name: Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
Labeler / Manufacturer: Kenvue Brands LLC
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20230228

FDA application: NDA021150

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 5 mg/1
- PSEUDOEPHEDRINE HYDROCHLORIDE: 120 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50580-719"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50580-719
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f1ecf9ba-1c03-7fb7-e053-2a95a90a875a