# Cetirizine Hydrochloride

NDC: 51672-2106
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Taro Pharmaceuticals U.S.A., Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20110520

FDA application: ANDA201546

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-2106"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-2106
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=67207357-5f8a-4424-9901-d2717a43cf1b