Active Ingredient: LEVOCETIRIZINE DIHYDROCHLORIDE
Proprietary Name: LEVOCETIRIZINE DIHYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A090362
Product Number: 001
Approval Date: Jan 31, 2013
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information