Active Ingredient: ESOMEPRAZOLE MAGNESIUM
Proprietary Name: ESOMEPRAZOLE MAGNESIUM
Dosage Form; Route of Administration: CAPSULE, DELAYED REL PELLETS; ORAL
Strength: EQ 20MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A209735
Product Number: 001
Approval Date: Apr 30, 2018
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information