Active Ingredient: PANTOPRAZOLE SODIUM
Proprietary Name: PANTOPRAZOLE SODIUM
Dosage Form; Route of Administration: FOR SUSPENSION, DELAYED RELEASE; ORAL
Strength: EQ 40MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A213725
Product Number: 001
Approval Date: Jun 30, 2020
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
