# cetirizine hydrochloride

NDC: 45802-919
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Padagis Israel Pharmaceuticals Ltd
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20071227

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:"45802-919"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=45802-919
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=91fe3ab8-c155-4482-9f06-f029d3563aad