FDA.reportPublic FDA data

NDC 0024-5823 - Jevtana

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
0024-5823
Package NDCs from labels
0024-5823-15
Manufacturer
Sanofi-Aventis U.S. LLC | Sanofi Winthrop Industrie | Sanofi-Aventis Deutschland GmbH
Effective date
2025-10-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Jevtana - Sanofi-Aventis U.S. LLC | Sanofi Winthrop Industrie | Sanofi-Aventis Deutschland GmbHSanofi-Aventis U.S. LLC | Sanofi Winthrop Industrie | Sanofi-Aventis Deutschland GmbH2025-10-07HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0024-5823-15Jevtana5.7 mL in 1 VIAL, GLASSINJECTION, SOLUTION, CONCENTRATE5.7 mL60 mg in 1.5mL27

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0024-5823JEVTANA (CABAZITAXEL) KIT [SANOFI-AVENTIS U.S. LLC]25Unmatched20240822_de3d9c26-572b-4ea4-9b2d-dd58a2b3e8fa.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
cabazitaxelACTIVE INGREDIENT51F690397JJEVTANA (CABAZITAXEL) KIT [SANOFI-AVENTIS U.S. LLC]13
cabazitaxelACTIVE MOIETY51F690397JJEVTANA (CABAZITAXEL) KIT [SANOFI-AVENTIS U.S. LLC]13
Polysorbate 80INACTIVE INGREDIENT6OZP39ZG8HJEVTANA (CABAZITAXEL) KIT [SANOFI-AVENTIS U.S. LLC]13