# Cetirizine hydrochloride

NDC: 70010-163
Generic name: Cetirizine hydrochloride
Labeler / Manufacturer: Granules Pharmaceuticals Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20220113

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:"70010-163"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70010-163
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d55dfce1-acef-3342-e053-2a95a90a4b83