# Cetirizine Hydrochloride Tablets,10 mg

NDC: 51655-842
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230207

FDA application: ANDA078933

## 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:"51655-842"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-842
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f756d3b1-d2e4-3705-e053-6294a90aa380