Active Ingredient: PANTOPRAZOLE SODIUM
Proprietary Name: PANTOPRAZOLE SODIUM
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: EQ 20MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A090074
Product Number: 001
Approval Date: Jan 19, 2011
Applicant Holder Full Name: TORRENT PHARMACEUTICALS LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
