# Cetirizine

NDC: 71610-123
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20180629

FDA application: ANDA078336

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71610-123"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71610-123
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4a45672b-67d3-4739-86ec-0a6696dd83d4
