# Allergy Relief

NDC: 68210-4159
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Prodose, Inc
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20210428

FDA application: ANDA077829

## 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:"68210-4159"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68210-4159
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e0e5f482-0282-410c-8c40-0a33ca4ea23a