Active Ingredient: PANTOPRAZOLE SODIUM
Proprietary Name: PANTOPRAZOLE SODIUM
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: EQ 40MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A211368
Product Number: 001
Approval Date: Mar 1, 2019
Applicant Holder Full Name: INGENUS PHARMACEUTICALS LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
