# Levocetirizine Dihydrochloride

NDC: 42571-122
Generic name: levocetirizine Dihydrochloride
Labeler / Manufacturer: Micro Labs Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20130930

FDA application: ANDA202046

## 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:"42571-122"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42571-122
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=717eb542-3a05-485e-be76-3930efb40d33