# levocetirizine dihydrochloride

NDC: 11673-847
Generic name: levocetirizine dihydrochloride
Labeler / Manufacturer: Target Corporation
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20181231

FDA application: ANDA210375

## Active ingredients

- LEVOCETIRIZINE DIHYDROCHLORIDE: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"11673-847"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11673-847
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7e933c85-96b0-b103-e26a-1aa8a1ded58e