# Cetirizine Hydrochloride

NDC: 71205-709
Generic name: Cetirizine Hydrochloride Tablets
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20181217

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:"71205-709"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-709
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=55b1738c-fa72-4cd1-a8e8-be41b12b593d