Foscarnet Sodium Injection, Solution
Product Images NDC 23155-771

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Foscarnet Sodium (NDC 23155-771). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals 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

Logo (Avet Logo)

FDA Label Image

Carton (Carton)

Foscarnet Sodium Injection 6,000 mg/250 mL (24 mg/mL) intravenous solution. The single-dose vial label includes usage instructions indicating dilution is required for peripheral intravenous infusion. Manufactured by Siegfried Hameln GmbH and labeled by Avet Pharmaceuticals Inc.*

FDA Label Image

Label (Label)

Label for Foscarnet Sodium Injection 6,000 mg per 250 mL (24 mg/mL) intravenous solution by Avet Pharmaceuticals Inc. The label specifies single-dose use, requiring dilution for peripheral intravenous infusion, with storage instructions and administration precautions noted. The product is made in Germany and distributed by Avet Pharma.*

FDA Label Image

Structure (Structure)

Chemical structure of foscarnet sodium showing phosphate and carboxylate groups coordinated with three sodium ions and six water molecules of hydration.*

* 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.