# Cetirizine Hydrochloride

NDC: 83939-0004
Generic name: Cetirizine Hydrochloride Tablets
Labeler / Manufacturer: VERITYRX, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20181217

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:"83939-0004"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83939-0004
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=42778a1c-6894-8646-e063-6294a90a6cb5