Zoledronic Acid Injection, Solution, Concentrate
Product Images NDC 67457-390

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Zoledronic Acid (NDC 67457-390). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Institutional 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

Structure (Image 01)

FDA Label Image

Formula (Image 02)

Formula (Image 02)
The text provides a figure (Figure 1) showing the proportion of complete responders by Day 10 in pooled studies of two drugs: Zoledronic Acid and Pamidronate. The proportion is represented as a percentage on the y-axis while the two drugs are named on the x-axis. The figure also includes numerical values on the y-axis, ranging from 0% to 100%, and a statistical significance (p-value) of 0.002. The sample size (n) for one of the drugs is also mentioned (n=86).*
FDA Label Image

Graph (Image 03)

Graph (Image 03)
This text describes the composition, storage, and dosage requirements of Zoledronic acid injection, a medication used for intravenous infusion. Each vial contains 4 mg of zoledronic acid, and the medication must be diluted before use. It can be stored in a refrigerated temperature range and must be used within 24 hours after dilution. The instructions warn not to mix the medication with calcium-containing infusion solutions. Dosage guidelines and the manufacturer, Mylan Institutional LLC, are also mentioned. No further details are available.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.