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:
Application Number: A077056
Product Number: 001
Approval Date: Aug 2, 2007
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information