# Cetirizine Hydrochloride Tablets, 5 mg

NDC: 25000-219
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: MARKSANS PHARMA LIMITED
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220113

FDA application: ANDA078933

## 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:"25000-219"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=25000-219
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=652b0c65-a3f2-4454-9cf2-51a3389282cc