# Allergy Relief

NDC: 21130-732
Generic name: levocetirizine dihydrochloride
Labeler / Manufacturer: Albertsons Companies
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20180630

FDA application: ANDA210375

## Active ingredients

- LEVOCETIRIZINE DIHYDROCHLORIDE: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"21130-732"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=21130-732
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e1a6932b-d076-6573-5b88-7b06c3a91681