Zoledronic Acid Injection
Product Images NDC 63323-961

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Zoledronic Acid (NDC 63323-961). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

Structural Formula (Zol12 0000 01)

Chemical structure of Zoledronic Acid showing its molecular components, including nitrogen atoms, phosphate groups, hydroxyl groups, and water of hydration.*

FDA Label Image

Figure 1 (Zol12 0000 02)

A bar graph showing the proportion of complete responders by day 10 in pooled hypertrophic cardiomyopathy (HCM) studies comparing Zoledronic acid Injection 4 mg (86 subjects) and Pamidronate 90 mg. The chart indicates higher complete response with Zoledronic acid, with a statistical significance of P=0.002.*

FDA Label Image

Figure (Zol12 0000 03)

Label for Zoledronic Acid Injection 4 mg per 5 mL (0.8 mg per mL) for intravenous infusion after dilution. The vial is single-dose, 5 mL, and must not be mixed with calcium-containing infusion solutions. Storage instructions specify 25°C (77°F) with permitted excursions. Manufactured for Fresenius Kabi USA, LLC in Lake Zurich, IL. Made in India.*

FDA Label Image

Figure (Zol12 0000 04)

Carton label for Zoledronic Acid Injection 4 mg per 5 mL (0.8 mg per mL) by Fresenius Kabi USA, LLC. The label includes dosage form as a single 5 mL single-dose vial for intravenous use, with directions emphasizing dilution before infusion and warnings against direct injection or mixing with calcium-containing solutions. Manufactured in India and distributed by Fresenius Kabi in Lake Zurich, IL.*

* 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.