# Cetirizine hydrochloride

NDC: 0615-8479
Generic name: Cetirizine hydrochloride
Labeler / Manufacturer: NCS HealthCare of KY, LLC dba Vangard Labs
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20220113

FDA application: ANDA209274

## 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:"0615-8479"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0615-8479
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b53d5e8a-a30c-4025-aa72-d2776a112e3e