# Cetirizine Hydrochloride

NDC: 30142-058
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: KROGER COMPANY
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20210308

FDA application: ANDA213557

## 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:"30142-058"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=30142-058
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b8b2af96-af48-5f63-e053-2995a90a7d7c