# Cetirizine Hydrochloride

NDC: 47335-343
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, CHEWABLE
Routes: ORAL
Marketing started: 20110909

FDA application: ANDA090142

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-343"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-343
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a4758152-97dd-4a27-b4d9-11178654b93e