Active Ingredient: DESLORATADINE
Proprietary Name: DESLORATADINE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078359
Product Number: 001
Approval Date: Nov 16, 2010
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information