Gamifant Injection
Product Images NDC 66658-510

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Gamifant (NDC 66658-510). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Swedish Orphan Biovitrum Ab (publ), 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

Gam01 0001 01

Gamifant 10 mg/2 mL (5 mg/mL) injection carton label for intravenous infusion by Swedish Orphan Biovitrum AB (publ). Label includes dosing information, storage instructions to refrigerate at 2°C to 8°C in the original carton, single-dose vial warning, and directions to dispense the enclosed Medication Guide to each patient. The label also lists inactive ingredients and notes no preservatives.*

FDA Label Image

Gam01 0001 02

Gamifant 100 mg/20 mL (5 mg/mL) injection carton label for intravenous infusion. The label states refrigeration requirements at 36°F to 46°F (2°C to 8°C), the need for dilution before administration, single-dose vial usage, and discarding unused portions. Manufactured by Swedish Orphan Biovitrum AB (publ) and Patheon Italia SpA, distributed by Sobi Inc. Includes warnings to see prescribing information and to dispense the enclosed medication guide.*

FDA Label Image

Gam01 0001 03

Packaging label for Gamifant (emapalumab-lzsg) Injection, 50 mg/10 mL (5 mg/mL), an intravenous infusion solution. The label includes storage instructions to refrigerate at 36°F to 46°F and warnings to protect from light and avoid freezing or shaking. Manufactured by Swedish Orphan Biovitrum AB, distributed by Sobi Inc. NDC 66658-505-01.*

* 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.