# cetirizine hydrochloride

NDC: 45802-974
Generic name: cetirizine hydrochloride
Labeler / Manufacturer: Padagis Israel Pharmaceuticals Ltd
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20080415

FDA application: ANDA090254

## 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:"45802-974"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=45802-974
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c2cf555d-986c-4e89-ac4f-938e92c418e2