# Cetirizine Hydrochloride

NDC: 45802-626
Generic name: Cetirizine hydrochloride
Labeler / Manufacturer: Padagis Israel Pharmaceuticals Ltd
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20080724

FDA application: ANDA078398

## 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:"45802-626"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=45802-626
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2f47dbc5-dfb4-425c-9fe4-777fa3c4e72e