FDA.reportPublic FDA data

NDC 67296-2047 - Pantoprazole Sodium

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
67296-2047
Package NDCs from labels
67296-2047-3, 67296-2047-7
Manufacturer
Redpharm drug
Effective date
2024-07-24
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Pantoprazole Sodium - Redpharm drugRedpharm drug2024-07-24HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67296-2047-3Pantoprazole Sodium30 in 1 BOTTLE, PLASTICTABLET, DELAYED RELEASE303
67296-2047-7Pantoprazole Sodium14 in 1 BOTTLETABLET, DELAYED RELEASE143

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67296-2047PANTOPRAZOLE SODIUM TABLET, DELAYED RELEASE [REDPHARM DRUG]32 package rows20240726_fa2bee95-97db-e651-e053-6294a90a72f5.zip