Product Images Kadcyla

View Photos of Packaging, Labels & Appearance

Product Label Images

The following 6 images provide visual information about the product associated with Kadcyla NDC 50242-088 by Genentech, Inc., such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

Chemical Structure - kadcyla 01

Chemical Structure - kadcyla 01

Figure 1 - kadcyla 02

Figure 1 - kadcyla 02

Figure 2 - kadcyla 03

Figure 2 - kadcyla 03

This is a survival analysis of patients (n=496) treated with ado-trastuzumab emtansine compared to lapatinib plus capecitabine. The analysis compares the duration of survival in months and shows the number of patients at risk along the way. The hazard ratio and p-value are estimated using a stratified Cox model and log-rank test, respectively. The text seems to be presenting a graph or a chart; however, only the text information extractable from the graphic is given, and the graph's image is not available.*

Figure 3 - kadcyla 04

Figure 3 - kadcyla 04

PRINCIPAL DISPLAY PANEL - 100 mg Vial Carton - kadcyla 05

PRINCIPAL DISPLAY PANEL - 100 mg Vial Carton - kadcyla 05

Kadcyla is a medication that requires intravenous infusion. This medication comes in a single-dose vial with a strength of 100 mg. Prior to administration, the medication must be reconstituted and diluted. Any unused portion of the product in the single-dose vial should be discarded. Kadcyla must be kept refrigerated. The manufacturer of this medication is Genentech and the product is identified by the National Drug Code (NDC) number 50242-088-01.*

PRINCIPAL DISPLAY PANEL - 160 mg Vial Carton - kadcyla 06

PRINCIPAL DISPLAY PANEL - 160 mg Vial Carton - kadcyla 06

Kadcyla® (ado-trastuzumab emtansine) is a medication that is administered through intravenous infusion only. It comes in a single-dose vial containing 160 mg per vial. The medication should be reconstituted and diluted before administration. Any unused portion should be discarded. The medication should be refrigerated and the given NDC code is 50242-087-01.*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.