# CETIRIZINE HYDROCHLORIDE

NDC: 69452-465
Generic name: CETIRIZINE HYDROCHLORIDE
Labeler / Manufacturer: Bionpharma Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20241020

FDA application: ANDA078862

## 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:"69452-465"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69452-465
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=831d4141-b3be-4d98-a372-9c4d57ad296c