Eraxis Injection, Powder, Lyophilized, For Solution
Product Images NDC 0049-2242

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Eraxis (NDC 0049-2242). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Roerig, 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

Chemical Structure (Eraxis 01)

Chemical structure diagram of anidulafungin, the active ingredient in ERAXIS injection powder, lyophilized, for intravenous use.*

FDA Label Image

Logo (Eraxis 02)

Packaging label showing the distributor information for ERAXIS (anidulafungin) injection, powder, lyophilized, for solution 100 mg/30 mL. The label states it is distributed by Roerig, a division of Pfizer Inc., New York, NY 10001.*

FDA Label Image

Premier Pro Logo (Eraxis 02a)

FDA Label Image

Principal Display Panel (100 mg Vial Label)

Label for Eraxis (anidulafungin) injection, powder, lyophilized, for solution, 100 mg per vial, for intravenous infusion only. The label includes storage instructions to refrigerate at 2° to 8°C and not to freeze, reconstitution directions with sterile water for injection, and dilution guidance. Distributed by Roerig, a division of Pfizer Inc., New York, NY.*

FDA Label Image

Principal Display Panel (100 mg Vial Carton)

The packaging label for ERAXIS (anidulafungin) injection, powder, lyophilized for solution, 100 mg per vial. The label indicates it is for intravenous infusion only and distributed by Roerig, a division of Pfizer Inc. Storage is recommended at 2°C to 8°C (36°F to 46°F), do not freeze. The label includes reconstitution instructions and specifies it contains one sterile single-dose vial per unit pack.*

* 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.