Zoledronic Acid Injection, Solution
Product Images NDC 67457-619

3 FDA label images from Mylan Institutional Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Zoledronic Acid (NDC 67457-619). 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.

Product Images & Figures Index

FDA Label Image

Stucture (Image 01)

Stucture (Image 01)
Chemical structure diagram of Zoledronic Acid showing its molecular framework with imidazole and phosphonic acid groups, consistent with the active ingredient Zoledronic Acid in the injection product by Mylan Institutional LLC.*
FDA Label Image

Therapeutic Response (Image 02)

Therapeutic Response (Image 02)
Two bar charts titled 'Therapeutic Response Over Time' and 'Serum Alkaline Phosphatase (SAP) Normalization Over Time' compare response rates over days 10, 28, 63, 91, and 182 between Zoledronic Acid Injection 5 mg/100 mL and Risedronate. The charts show percentage rates on the y-axis with Zoledronic Acid achieving higher rates at each time point, marked with statistical significance.*
FDA Label Image

Carton 0.05mg (Image 03)

Carton 0.05mg (Image 03)
Packaging label for Zoledronic Acid Injection 5 mg/100 mL (0.05 mg/mL) solution for intravenous infusion. The label includes dosing and storage information, manufacturer details (Mylan Institutional LLC, Rockford, IL, USA), and instructions for single-dose vial use. The label prominently displays the NDC 67457-619-10 and the Mylan logo.*

* 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.