Active Ingredient: IMATINIB MESYLATE
Proprietary Name: IMATINIB MESYLATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 100MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A078340
Product Number: 001
Approval Date: Dec 3, 2015
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information