Dexamethasone Sodium Phosphate Injection, Solution
Product Images NDC 63323-516

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Dexamethasone Sodium Phosphate (NDC 63323-516). 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

Dex12 0003 01

Chemical structure of dexamethasone sodium phosphate depicting the molecular arrangement with atoms and bonds, including fluorine and phosphate groups as part of the steroid framework.*

FDA Label Image

Dex12 0003 02

FDA Label Image

Dex12 0003 03

Label for Dexamethasone Sodium Phosphate Injection, USP, 10 mg per mL solution. The label states the product is for intramuscular or intravenous use, single dose vial, preservative-free, and discard unused portion. It is labeled for prescription use only by Fresenius Kabi USA, LLC.*

FDA Label Image

Dex12 0003 04

Label for Dexamethasone Sodium Phosphate injection, USP 10 mg per mL solution, single-dose vial of 1 mL for intramuscular or intravenous use. The label shows dosage strength, route, quantity of 25 vials, and the labeler Fresenius Kabi USA, LLC. It includes a barcode and NDC 63323-506-01.*

FDA Label Image

Dex12 0003 05

Dexamethasone Sodium Phosphate Injection, USP label showing 100 mg per 10 mL (10 mg per mL) solution. The label indicates administration routes as intramuscular (IM) or intravenous (IV) use, prescription only, with a 10 mL multiple dose vial, labeled by Fresenius Kabi USA, LLC.*

FDA Label Image

Dex12 0003 06

Label for Dexamethasone Sodium Phosphate Injection, USP, 100 mg per 10 mL (10 mg per mL) multiple dose vial. The package contains 10 vials, each 10 mL. The product is for intravenous or intramuscular use and is labeled by Fresenius Kabi USA, LLC. The label includes NDC 63323-516-10, usage and 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.