Fosphenytoin Sodium Injection, Solution
Product Images NDC 25021-798

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Fosphenytoin Sodium (NDC 25021-798). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sagent Pharmaceuticals, 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 (Fos0g 0000 01)

Chemical structure of Fosphenytoin Sodium showing its molecular framework including phenyl groups, amide, phosphate groups, and sodium ions as part of the compound.*

FDA Label Image

Figure 1 (Fos0g 0000 02)

A pharmacokinetic graph showing plasma unbound phenytoin concentration (µg/mL) over time (hours) after start of infusion, with multiple plotted curves representing different conditions or subjects during the first 2 hours. An inset graph depicts plasma unbound phenytoin concentration over a longer duration (0 to 96 hours) following infusion start.*

FDA Label Image

Package Label – Principal Display Panel – Vial Label (Fos0g 0000 03)

Label for Fosphenytoin Sodium Injection, USP 100 mg PE per 2 mL (50 mg PE per mL) by Sagent Pharmaceuticals. This single-dose 2 mL vial contains fosphenytoin sodium equivalent to 150 mg sodium, 100 mg phenytoin. It is for intramuscular or intravenous use and includes a barcode and manufacturing details.*

FDA Label Image

Package Label – Principal Display Panel – Vial Label (Fos0g 0000 04)

Label for Fosphenytoin Sodium Injection, USP, 50 mg PE per mL (500 mg PE per 10 mL) in a 10 mL single-dose vial. The injection is for intramuscular or intravenous use, produced by Sagent Pharmaceuticals. The label includes storage instructions and a barcode.*

* 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.