Active Ingredient: PANTOPRAZOLE SODIUM
Proprietary Name: PANTOPRAZOLE SODIUM
Dosage Form; Route of Administration: INJECTABLE; INTRAVENOUS
Strength: EQ 40MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A205675
Product Number: 001
Approval Date: Mar 30, 2016
Applicant Holder Full Name: EUGIA PHARMA SPECIALITIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information