Xgeva Injection
Product Images NDC 55513-730

2 FDA label images from Amgen, Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Xgeva (NDC 55513-730). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amgen, 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

Figure 1 (Xgeva 01)

Figure 1 (Xgeva 01)
Chart titled 'Corrected Serum Calcium by Visit in Responders (Median and Interquartile Range)' showing serum calcium levels over study days for 23 responders receiving 120 mg denosumab. The graph plots corrected calcium levels (mmol/L and mg/dL) decreasing from baseline through day 57 with error bars representing interquartile ranges.*
FDA Label Image

Principal Display Panel 1 X 120 mg Single Dose Vialndc 55513-730-01amgen®xgeva®(denosumab)120 mg/1.7 mL(70 mg/ml)injectionfor Subcutaneous Use Only120 mg/1.7 mLsingle Dose Vial. Discard Unused Portion.sterile Solution – No Preservativerefrigerate At 2° To 8°c (36° To 46°f).do Not Freeze. Avoid Excessive Shaking. Protect From Direct Light.manufactured By: Amgen Inc. Thousand Oaks, Ca 91320-1799u.s. License No. 1080product Of Singapore (Xgeva 03)

Principal Display Panel 1 X 120 mg Single Dose Vialndc 55513-730-01amgen®xgeva®(denosumab)120 mg/1.7 mL(70 mg/ml)injectionfor Subcutaneous Use Only120 mg/1.7 mLsingle Dose Vial. Discard Unused Portion.sterile Solution – No Preservativerefrigerate At 2° To 8°c (36° To 46°f).do Not Freeze. Avoid Excessive Shaking. Protect From Direct Light.manufactured By: Amgen Inc. Thousand Oaks, Ca 91320-1799u.s. License No. 1080product Of Singapore (Xgeva 03)
XGEVA 120 mg/1.7 mL injection vial label, containing denosumab, manufactured by Amgen, Inc. This packaging label identifies the product as a single-dose vial for subcutaneous injection, with detailed formulation information and storage instructions. The NDC number 55513-730-01 is displayed on the label.*

* 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.