# Allergy Relief

NDC: 83324-091
Generic name: Cetirizine hydrochloride
Labeler / Manufacturer: CHAIN DRUG MARKETING ASSOCIATION, INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20240816

FDA application: ANDA209274

## 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:"83324-091"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83324-091
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6eb22b5a-ff30-44f8-aca2-3f73614515a8