# Cetirizine Hydrochloride (Allergy)

NDC: 57483-190
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: INNOVUS PHARMACEUTICALS, INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250428

FDA application: ANDA090760

## 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:"57483-190"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57483-190
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=89db2c96-62f6-4e75-8f0d-321b44094c60