# Cetirizine Hydrochloride

NDC: 0781-5283
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, CHEWABLE
Routes: ORAL
Marketing started: 20080214

FDA application: ANDA078692

## 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:"0781-5283"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-5283
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=817d07cf-5e31-421f-9e95-943bae01f5b0