# Cetirizine hydrochloride

NDC: 23155-929
Generic name: Cetirizine hydrochloride
Labeler / Manufacturer: Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20250301

FDA application: ANDA078876

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 5 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"23155-929"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-929
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a9b21d71-106e-4bd5-aaab-9254c8a44e0d