Fosphenytoin Injection, Solution
Product Images NDC 63323-403

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Fosphenytoin (NDC 63323-403). 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.

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Fosphenytoin Sodium Injection is a medication used for intramuscular or intravenous use, and is offered in 10 mL single dose vials with each vial containing 500 mg PE per 10 mL (50 mg PE per mL). This medication is sterile, and is refrigerated at 2°to 89 (36° to 46°F). Each vial contains Fosphenytoin sodium 750mg equivalent to 500mg phenytoin sodium. The usual dosage and administration should be seen in the package insert. Note that the administration of this medication differs from parenteral phenytoin.*

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Fosphenytoin Sodium Injection, USP is a sterile solution with 500 mg Phenitoyn Sodium equivalent per 10 mL (50 mg per mL) for intravenous or intramuscular use. Each 1010 mL vial contains 750 mg equivalent of 500 mg Phenytoin Sodium; tromethamine (TRI) as a buffer; hydrochloric acid; or sodium hydroxide to adjust the pH to 8.6 109 and sufficient water for injection. Dosage instructions are provided in the package insert, and administration differs from parenteral phenytoin. The product should be refrigerated at 2° to 8°C (36° to 46°F). The container closure does not contain natural rubber latex. LOT/EXP number is 42798F 010363323403106.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.