# LEVOCETIRIZINE DIHYDROCHLORIDE

NDC: 71335-0418
Generic name: LEVOCETIRIZINE DIHYDROCHLORIDE
Labeler / Manufacturer: Bryant Ranch Prepack
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

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-0418"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-0418
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1b593c65-2866-45d9-9c94-ac181f4cbc51