Zaltrap Solution, Concentrate
Product Images NDC 0024-5841

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Zaltrap (NDC 0024-5841). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sanofi-aventis U.s. Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Figure 1 (Zaltrap 01)

A Kaplan-Meier survival curve chart comparing the probability of surviving over time (in months) between two groups: Placebo/Folfiri and ZALTRAP/Folfiri. The chart displays a higher survival probability for the ZALTRAP/Folfiri group over approximately 36 months, with censored data points indicated by specific symbols. Below the graph, numbers at risk for each group are shown at various time intervals.*

FDA Label Image

Principal Display Panel (100 mg/4 mL Vial Carton)

Packaging label for ZALTRAP (ziv-aflibercept) 100 mg/4 mL injection solution for intravenous infusion. The single-dose vial label highlights it is for intravenous use only, hyperosmotic and must be diluted. The label provides storage instructions, manufacturer details (sanofi-aventis U.S. LLC), and includes an NDC number 0024-5840-01.*

FDA Label Image

Principal Display Panel (200 mg/8 mL Vial Carton)

ZALTRAP (ziv-aflibercept) 200 mg/8 mL (25 mg/mL) injection for intravenous infusion. The label is for a single-dose vial to be diluted prior to use and is for intravenous administration only. It includes storage instructions to refrigerate at 2-8°C and warnings to discard unused portions. The labeler is sanofi-aventis U.S. LLC, with details on manufacturing location and trademark information.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.