# CABINET Allergy Relief

NDC: 68210-0119
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Spirit Pharmaceutical LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20191025

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:"68210-0119"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68210-0119
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e49c3c91-aab8-478e-97fa-04ed06180021