FDA.reportPublic FDA data

NDC 67296-1187 - 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
67296-1187
Package NDCs from labels
67296-1187-3
Manufacturer
RedPharm Drug
Effective date
2024-07-15
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
PANTOPRAZOLE SODIUM - RedPharm DrugRedPharm Drug2024-07-15HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67296-1187-3PANTOPRAZOLE SODIUM30 in 1 BOTTLETABLET, DELAYED RELEASE301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67296-1187PANTOPRAZOLE SODIUM (PANTOPRAZOLE) TABLET, DELAYED RELEASE [REDPHARM DRUG]11 package rows20240716_1d51ffeb-21ef-e2b5-e063-6294a90a00dd.zip