Zoledronic Acid Injection, Solution
Product Images NDC 71288-806

View Photos of 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 71288-806). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meitheal Pharmaceuticals 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

Structural Formula (Zol10 0002 01)

Structural Formula (Zol10 0002 01)
Chemical structure of Zoledronic Acid, showing its molecular configuration with phosphonate groups and an imidazole ring.*
FDA Label Image

Figure 2 (Zol10 0002 02)

Figure 2 (Zol10 0002 02)
Two bar charts showing the therapeutic response and serum alkaline phosphatase (SAP) normalization rates over time for Zoledronic Acid and Risedronate. The charts compare response rates at 10, 28, 63, 91, and 182 days, indicating statistical significance at several time points.*
FDA Label Image

Vial Label (Zol10 0002 03)

Vial Label (Zol10 0002 03)
Label for Zoledronic Acid Injection 5 mg/100 mL (0.05 mg/mL) sterile solution for intravenous infusion, in a 100 mL single-dose bottle. The label includes dosage and administration instructions, storage conditions, and a note about the container closure made with natural rubber latex. It is manufactured for Meitheal Pharmaceuticals Inc.*
FDA Label Image

Carton (Zol10 0002 04)

Carton (Zol10 0002 04)
Packaging label for Zoledronic Acid Injection 5 mg per 100 mL (0.05 mg per mL) sterile solution for intravenous infusion. The label shows a 1 x 100 mL single-dose bottle with storage, administration, and mixing instructions. The labeler is Meitheal Pharmaceuticals Inc., and the NDC number is 71288-806-51.*

* 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.