# levocetirizine dihydrochloride

NDC: 68788-7934
Generic name: levocetirizine dihydrochloride
Labeler / Manufacturer: Preferred Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210615

FDA application: ANDA203646

## Active ingredients

- LEVOCETIRIZINE DIHYDROCHLORIDE: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-7934"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-7934
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8f308352-5854-409e-8bf7-bc9958cc3c5e