# Cetirizine Hydrochloride (Allergy)

NDC: 21130-098
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Better Living Brands, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230519

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:"21130-098"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=21130-098
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f7e16d96-4f23-cbca-e053-6394a90aef4e