Zoledronic Acid Injection, Solution, Concentrate
Product Images NDC 43598-233

View Photos of 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 43598-233). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr. Reddy's Laboratories Inc., 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

Carton (Carton)

Carton (Carton)
The packaging label for Zoledronic Acid Injection 4 mg/5 mL (0.8 mg/mL) sterile concentrate for intravenous infusion by Dr. Reddy's Laboratories Inc. The label indicates it is a 5 mL single-dose vial concentrate that must be diluted before use and is not for direct injection. The label includes NDC 43598-233-11, barcode, storage instructions, and manufacturer details, noting the product is made in India.*
FDA Label Image

Graph (Graph)

Graph (Graph)
A bar graph titled 'Proportion of Complete Responders by Day 10 In Pooled HCM Studies' comparing Zoledronic Acid Injection 4 mg (n=86) and Pamidronate 90 mg (n=99). The y-axis represents percentage of complete responders from 0% to 100%. Zoledronic Acid shows a higher response rate approaching 85%, while Pamidronate shows a response rate near 65%. Statistical significance is indicated with P=0.002.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of Zoledronic Acid depicting its molecular framework with nitrogen-containing rings and phosphonate groups.*

* 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.