# Cetirizine Hydrochloride

NDC: 76162-009
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: TOPCO ASSOCIATES LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20240606

FDA application: ANDA213557

## 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:"76162-009"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76162-009
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f4ba3e0c-e6b3-2596-e053-2a95a90ab850