Foscarnet Sodium Injection, Solution
Product Images NDC 0143-9192

View Photos of 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 Foscarnet Sodium (NDC 0143-9192). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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

Structural Formula (Foscarnet 001)

Structural Formula (Foscarnet 001)
Chemical structure diagram of foscarnet sodium, showing the sodium ions (Na+) and water molecules (H2O) associated with the phosphate group.*
FDA Label Image

Logo (Foscarnet 002)

FDA Label Image

Bottle Label (Foscarnet 003)

Bottle Label (Foscarnet 003)
Label for Foscarnet Sodium Injection 24 mg/mL (6000 mg per 250 mL) by Hikma Pharmaceuticals USA Inc. The label includes NDC 0143-9192-01, indicates it is for central intravenous infusion only and must be diluted for peripheral intravenous infusion. Additional storage and administration instructions are printed, including temperature control and dilution requirements.*
FDA Label Image

Carton (Foscarnet 004 1)

Carton (Foscarnet 004 1)
Packaging label for Foscarnet Sodium Injection 24 mg/mL (6000 mg per 250 mL) by Hikma Pharmaceuticals USA Inc. The label shows the product name, strength, and volume, indicating it is for intravenous use and must be diluted for peripheral intravenous infusion. Manufacturer is Beijing Scicure Pharmaceutical Co., Ltd., with distribution by Hikma Pharmaceuticals USA Inc. The label also includes storage instructions and administration precautions.*

* 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.