Dexamethasone Sodium Phosphate Injection
Product Images NDC 55150-304

3 FDA label images from Eugia Us Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dexamethasone Sodium Phosphate (NDC 55150-304). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eugia Us 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

Package Label-principal Display Panel (10 mg per mL)

Package Label-principal Display Panel (10 mg per mL)
Dexamethasone Sodium Phosphate Injection, USP 10 mg/mL, 1 mL single-dose vial. The label indicates it is preservative-free, for intravenous or intramuscular use only, and Rx only. Labeler is Eugia US LLC, manufactured in India for AuroMedics Pharma LLC, E. Windsor, NJ.*
FDA Label Image

Package Label-principal Display Panel (10 mg per mL)

Package Label-principal Display Panel (10 mg per mL)
Packaging label for Dexamethasone Sodium Phosphate Injection, USP, 10 mg per mL. The label indicates single-dose vials of 1 mL for intravenous or intramuscular use. Distributed by AuroMedics Pharma LLC, the label includes dosage and storage information, highlighting that the product is preservative free and sterile.*
FDA Label Image

Dexamethasone Sodium Phosphate Chemical Structure (Dexamethasone Str)

Dexamethasone Sodium Phosphate Chemical Structure (Dexamethasone Str)
Chemical structure of dexamethasone sodium phosphate, the active ingredient in the product. The diagram shows the steroid backbone with functional groups including phosphate and hydroxyl groups.*

* 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.