# cetirizine hydrochloride

NDC: 71610-862
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
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:"71610-862"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71610-862
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=25db4ca0-0c25-f3b6-e063-6394a90a8851