FDA.reportPublic FDA data

NDC 50242-009 - TNKase

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
50242-009
Package NDCs from labels
50242-009-01
Manufacturer
Genentech, Inc. | Genentech, Inc. (Hillsboro) | Genentech, Inc. (Oceanside)
Effective date
2025-12-15
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
TNKase - Genentech, Inc. | Genentech, Inc. (Hillsboro) | Genentech, Inc. (Oceanside)Genentech, Inc. | Genentech, Inc. (Hillsboro) | Genentech, Inc. (Oceanside)2025-12-15HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50242-009-01TNKase1 in 1 CARTONINJECTION, POWDER, LYOPHILIZED,25 mg in 5mL4
50242-009-01TNKase5 mL in 1 VIAL, SINGLE-USEINJECTION, POWDER, LYOPHILIZED,5 mL25 mg in 5mL4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50242-009TNKASE (TENECTEPLASE) KIT [GENENTECH, INC.]3Unmatched20250412_e647640d-c395-4b4b-a0be-1162f9c21d84.zip