# levocetirizine dihydrochloride

NDC: 43598-735
Generic name: levocetirizine dihydrochloride
Labeler / Manufacturer: Dr. Reddy's Laboratories Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20180312

FDA application: ANDA210375

## 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:"43598-735"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-735
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1f722b84-08de-7e6a-41ac-2c9d9bb9fb43