# CETIRIZINE HYDROCHLORIDE

NDC: 61037-479
Generic name: CETIRIZINE HYDROCHLORIDE
Labeler / Manufacturer: BAJAJ MEDICAL, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20230912

FDA application: ANDA090191

## 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:"61037-479"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=61037-479
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3b5908f1-faba-c317-e063-6294a90aa8a7