# Levocetirizine Dihydrochloride

NDC: 69230-321
Generic name: Levocetirizine Dihydrochloride
Labeler / Manufacturer: Camber Consumer Care Inc
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20201028

FDA application: ANDA213513

## 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:"69230-321"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69230-321
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=be72dafb-62ae-40b2-874f-1d8920fad19d