# levocetirizine dihydrochloride

NDC: 68071-2406
Generic name: levocetirizine dihydrochloride
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20140909

FDA application: ANDA203646

## 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:"68071-2406"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-2406
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c2dbf151-5b3d-5dfb-e053-2995a90a4c19