# Levocetirizine Dihydrochloride

NDC: 31722-551
Generic name: Levocetirizine Dihydrochloride
Labeler / Manufacturer: Camber 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:"31722-551"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-551
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dd407f8f-140d-489f-b8c5-f6602d87e247