Allopurinol Injection, Powder, Lyophilized, For Solution
Product Images NDC 65219-380

4 FDA label images from Fresenius Kabi Usa, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Allopurinol (NDC 65219-380). 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 (All0d 0002 01)

Structural Formula (All0d 0002 01)
Chemical structure depicting the molecular arrangement of Allopurinol sodium, illustrating the bicyclic purine analog with nitrogen and oxygen atoms, along with the sodium ion (Na+).*
FDA Label Image

Logo (All0d 0002 02)

FDA Label Image

Principal Display Panel – Shelf Carton (All0d 0002 03)

Principal Display Panel – Shelf Carton (All0d 0002 03)
Packaging label for Allopurinol injection, 500 mg per vial, for intravenous infusion. The label indicates a single-dose vial, sterile, Rx only, manufactured by Fresenius Kabi USA, LLC. The label includes preparation instructions, storage conditions at 20°C to 25°C, and a barcode with NDC 65219-380-30. The product is made in India.*
FDA Label Image

Principal Display Panel – Vial Label (All0d 0002 04)

Principal Display Panel – Vial Label (All0d 0002 04)
Label for Allopurinol for Injection 500 mg/vial, a lyophilized powder for intravenous infusion by Fresenius Kabi USA, LLC. The single-dose vial requires reconstitution with sterile water before administration. Storage is specified at controlled room temperature (20°C to 25°C). The label includes a barcode, manufacturing information, and usage instructions.*

* 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.