Zoledronic Acid Injection, Solution, Concentrate
Product Images NDC 54288-183

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Zoledronic Acid (NDC 54288-183). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bpi Labs 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.

FDA Label Image

Struture (6565)

Chemical structure of zoledronic acid, showing its molecular arrangement including a nitrogen-containing ring and two phosphonic acid groups, as represented in the image.*

FDA Label Image

Diagram (Diagram)

A bar graph titled 'Proportion of Complete Responders by Day 10 in Pooled HCM Studies' compares the percentage of complete responders between Zoledronic Acid Injection 4 mg and Pamidronate 90 mg. The Zoledronic Acid bar is higher, indicating a higher response rate, with a statistical significance noted (P=0.002).*

FDA Label Image

Carton (Zoledronic Acid Vial Carton)

Packaging label for Zoledronic Acid Injection 4 mg/5 mL (0.8 mg/mL) concentrate for intravenous infusion, manufactured by BPI Labs LLC. The carton includes usage instructions, storage conditions, and a barcode. The label states Rx only and indicates a single 5 mL vial is included.*

FDA Label Image

Vial Label (Zoledronic Acid Vial Label)

Label for Zoledronic Acid Injection 4 mg/5 mL (0.8 mg/mL) solution concentrate for intravenous use, single dose vial. Manufactured for BPI Labs LLC. Includes storage instructions, dilution requirements, and warnings not to mix with calcium-containing infusion solutions.*

* 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.