# Levocetirizine Dihydrochloride

NDC: 49035-492
Generic name: Levocetirizine Dihydrochloride
Labeler / Manufacturer: Walmart Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20190726

FDA application: ANDA210375

## 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:"49035-492"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49035-492
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=82da5fa1-3633-2c48-32b9-d15482f308a1