# Cetirizine Hydrochloride (Allergy)

NDC: 30142-172
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: KROGER COMPANY
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210315

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:"30142-172"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=30142-172
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b92d959d-dd35-b2a3-e053-2995a90af3ff