Zoledronic Acid Injection, Solution
Product Images NDC 43598-331

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 43598-331). 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.

FDA Label Image

Carton (Carton)

Carton (Carton)
Packaging label for Zoledronic Acid Injection 5 mg/100 mL (0.05 mg/mL) intravenous solution by Dr.Reddy's Laboratories Inc. The label indicates a single 100 mL sterile solution bottle for intravenous infusion. Instructions highlight not mixing with calcium-containing solutions and advise administration as a single intravenous infusion through a separate vented line. The label includes dosing and storage information, barcodes, and the Novaplus trademark.*
FDA Label Image

Figure2 (Figure2)

Figure2 (Figure2)
Two bar graphs comparing therapeutic response rates and serum alkaline phosphatase (SAP) normalization rates over time in days for Zoledronic Acid injection versus Risedronate. The graphs show increasing percentages over 182 days, with Zoledronic Acid demonstrating higher response and SAP normalization rates at measured intervals. Statistical significance is noted with asterisks (P < 0.001).*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram of Zoledronic Acid, showing its molecular arrangement including a pyrazole ring and phosphonic acid groups, corresponding to the active ingredient in the specified drug product.*

* 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.