# Cetirizine Hydrochloride

NDC: 65162-045
Generic name: Cetirizine
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20100121

FDA application: ANDA078780

## 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:"65162-045"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65162-045
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=214936a2-adc4-422a-a8fe-4c3ce9e01f36