# Cetirizine Hydrochloride

NDC: 68788-8435
Generic name: Cetirizine Hydrochloride Tablets
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230427

FDA application: ANDA078343

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-8435"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8435
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=14a885e5-5e75-4a18-b5bc-6aaa748712db