Dexamethasone Sodium Phosphate Injection, Solution
Product Images NDC 70121-1399

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dexamethasone Sodium Phosphate (NDC 70121-1399). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals 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

1 (Dexamethasone Sodium Phosphate Injection Usp 10 mg 1)

Chemical structure diagram of dexamethasone sodium phosphate showing its steroid backbone with functional groups including hydroxyl, ketone, fluorine substituent, and the sodium phosphate moiety.*

FDA Label Image

1 (Dexamethasone Sodium Phosphate Injection Usp 10 mg 2)

Label for Dexamethasone Sodium Phosphate Injection, USP 10 mg/mL single-dose vial by Amneal Pharmaceuticals LLC. The label states it is for intramuscular or intravenous use, preservative free, and includes storage instructions to keep between 20°C to 25°C and protect from light. NDC 70121-1399. Rx only.*

FDA Label Image

1 (Dexamethasone Sodium Phosphate Injection Usp 10 mg 3)

Packaging label for Dexamethasone Sodium Phosphate Injection, USP 10 mg/mL by Amneal Pharmaceuticals LLC. The label indicates the product is an injection solution for intramuscular or intravenous use only, supplied as 25 single-dose vials of 1 mL each. The label includes storage instructions, usage warnings, and identifies the manufacturer as Amneal Pharmaceuticals Pvt. Ltd., India, with distribution by Amneal Pharmaceuticals LLC, New Jersey, USA.*

* 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.