# Levocetirizine Dihydrochloride

NDC: 0093-7701
Generic name: Levocetirizine Dihydrochloride
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20110906

FDA application: ANDA090199

## 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:"0093-7701"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-7701
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4f43d057-cba8-4366-86ba-4be361e4c71f