Kalbitor Injection, Solution
Product Images NDC 47783-101

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Kalbitor (NDC 47783-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Takeda Pharmaceuticals America, 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

Takeda Logo (Kalbitor 03)

Kalbitor 10 mg/mL injection solution for subcutaneous use packaging label. The label shows the product name Kalbitor prominently at top, with active ingredient ecallantide below. The label includes the strength 10 mg/mL and indicates that it is for human prescription use. Takeda Pharmaceuticals America, Inc. is listed as the labeler. The label design features a blue and white color scheme with Takeda branding.*

FDA Label Image

Principal Display Panel (10 mg/mL Vial Carton)

Kalbitor injection solution, 10 mg/mL (ecallantide) packaging label for subcutaneous use, containing 3 vials. Produced by Takeda Pharmaceuticals America, Inc. The label includes storage instructions to keep refrigerated, protect from light, and warnings against freezing. Dosage information indicates 30 mg requiring 3 vials. Additional product details and contact information are also present.*

FDA Label Image

Principal Display Panel (10 mg/mL Vial Bottle)

Label for Kalbitor injection, an ecallantide solution at 10 mg/mL strength, intended for single-dose use and subcutaneous administration. The label indicates prescription-only status and is from Takeda Pharmaceuticals U.S.A., Inc. The NDC shown is 47783-101-01.*

* 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.