# Cetirizine Hydrochloride

NDC: 63629-4914
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20091001

FDA application: ANDA077829

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-4914"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-4914
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ddec7d64-ab3d-4ddd-9bcd-b7f4d2b46be7