# Cetirizine Hydrochloride

NDC: 55289-995
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20071227

FDA application: ANDA077498

## 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:"55289-995"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55289-995
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a7da81e1-8865-45c9-83c7-32fb8032ca2e