# Cetirizine Hydrochloride

NDC: 51655-801
Generic name: Cetirizine Hydrochloride Tablets
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230125

FDA application: ANDA078343

## 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:"51655-801"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-801
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f70886af-a8a4-63a0-e053-6294a90a2d2c