# LEVOCETIRIZINE DIHYDROCHLORIDE

NDC: 68462-346
Generic name: levocetirizine dihydrochloride
Labeler / Manufacturer: Glenmark Pharmaceuticals Inc., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20110225

FDA application: ANDA090385

## 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:"68462-346"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-346
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=60ae7e0e-281c-40a3-a0d3-259b843ddaaa