Zoledronic Acid
Product Images NDC 17478-327

4 FDA label images from Akorn · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Zoledronic Acid (NDC 17478-327). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Akorn, 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

Zol0h 0006 01

Zol0h 0006 01
Chemical structure diagram of Zoledronic Acid showing its molecular arrangement including phosphate groups and imidazole ring, with three associated water molecules (trihydrate form).*
FDA Label Image

Zol0h 0006 02

Zol0h 0006 02
A bar chart illustrating the proportion of complete responders by day 10 in pooled HCM studies. The chart compares Zoledronic Acid Injection 4 mg (n=86) with Pamidronate 90 mg (n=99), indicating a higher response rate for Zoledronic Acid. A p-value of 0.002 is shown between the bars.*
FDA Label Image

Zol0h 0006 03

Zol0h 0006 03
Label for Zoledronic Acid Injection 4 mg/5 mL (0.8 mg/mL) sterile concentrate in a 5 mL single-dose vial by Akorn, Inc. The label states the product is for intravenous infusion after dilution, not for direct injection, and must be diluted before use. Storage instructions and manufacturer information from Fresenius Kabi Austria GmbH are included.*
FDA Label Image

Zol0h 0006 04

Zol0h 0006 04
Packaging label for Zoledronic Acid Injection 4 mg/5 mL (0.8 mg/mL) sterile concentrate by Akorn. The label states it is for intravenous infusion after dilution and comes in a 1 x 5 mL single-dose vial. The label includes instructions that the dose must be diluted and not directly injected, with warnings about not mixing with calcium-containing infusion solutions. The label also notes the product is Rx only and provides the NDC 17478-327-05.*

* 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.