# levocetirizine dihydrochloride

NDC: 11822-5252
Generic name: levocetirizine dihydrochloride
Labeler / Manufacturer: Rite Aid Corporation
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20200215

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:"11822-5252"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11822-5252
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fafc8149-d59a-1253-ae79-f33a088e3769