Active Ingredient: PANTOPRAZOLE SODIUM
Proprietary Name: PROTONIX
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: EQ 20MG BASE
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N020987
Product Number: 002
Approval Date: Jun 12, 2001
Applicant Holder Full Name: WYETH PHARMACEUTICALS LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
