# Levocetirizine Dihydrochloride

NDC: 72789-023
Generic name: Levocetirizine Dihydrochloride
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20120629

FDA application: ANDA091264

## Active ingredients

- LEVOCETIRIZINE DIHYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72789-023"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-023
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=57c7c673-790c-4158-87ca-7d8fb68c4286