# Cetirizine Hydrochloride (Allergy)

NDC: 16714-799
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: NorthStar Rx LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20150805

FDA application: ANDA090760

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16714-799"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16714-799
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c9d1e26f-c95a-4991-95fa-9ed6ed484fe2