# CETIRIZINE HYDROCHLORIDE

NDC: 57237-358
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20251111

FDA application: ANDA091327

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57237-358"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57237-358
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=06cdcbe0-6c7c-4b91-8158-08ef2e0876dc