# Levocetirizine Dihydrochloride

NDC: 51655-148
Generic name: Levocetirizine Dihydrochloride
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20221004

FDA application: ANDA091264

## Active ingredients

- LEVOCETIRIZINE DIHYDROCHLORIDE: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-148"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-148
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f2b458d6-ac10-0fed-e053-2a95a90a0f9c