Active Ingredient: OMEPRAZOLE MAGNESIUM
Proprietary Name: OMEPRAZOLE MAGNESIUM
Dosage Form; Route of Administration: CAPSULE, DELAYED RELEASE; ORAL
Strength: EQ 20MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A213201
Product Number: 001
Approval Date: Apr 28, 2023
Applicant Holder Full Name: AUROBINDO PHARMA LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information
