# LEVOCETIRIZINE DIHYDROCHLORIDE

NDC: 33342-200
Generic name: LEVOCETIRIZINE DIHYDROCHLORIDE
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160111

FDA application: ANDA205564

## Active ingredients

- LEVOCETIRIZINE DIHYDROCHLORIDE: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"33342-200"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-200
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8a3c06a5-4a9a-4205-8ae7-c58efeb73c58