Dexamethasone Sodium Phosphate Injection, Solution
Product Images NDC 70121-1452

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Dexamethasone Sodium Phosphate (NDC 70121-1452). 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

Structure (Dexamethasone Sodium Phosphate Injection Usp 4 mg 1)

Structure (Dexamethasone Sodium Phosphate Injection Usp 4 mg  1)
Chemical structure of dexamethasone sodium phosphate, showing its steroid backbone with associated functional groups including hydroxyl, fluorine, and phosphate moieties.*
FDA Label Image

1 (Dexamethasone Sodium Phosphate Injection Usp 4 mg 2)

1 (Dexamethasone Sodium Phosphate Injection Usp 4 mg  2)
Label for Dexamethasone Sodium Phosphate Injection USP, 4 mg/mL, single-dose vial. The injection is intended for intramuscular or intravenous use and is labeled Rx only. The label includes storage instructions, manufacturer Amneal Pharmaceuticals LLC information, and lot/expiration area.*
FDA Label Image

2 (Dexamethasone Sodium Phosphate Injection Usp 4 mg 3)

2 (Dexamethasone Sodium Phosphate Injection Usp 4 mg  3)
The packaging label for Dexamethasone Sodium Phosphate Injection, USP 4 mg/mL by Amneal Pharmaceuticals LLC. The label indicates it is a solution for injection available in 25 single-dose vials of 1 mL each. It is intended for intravenous, intramuscular, intra-articular, soft tissue, or intralesional use. Storage and handling instructions, manufacturer details, and a barcode are also visible.*
FDA Label Image

3 (Dexamethasone Sodium Phosphate Injection Usp 4 mg 4)

3 (Dexamethasone Sodium Phosphate Injection Usp 4 mg  4)
Label for Dexamethasone Sodium Phosphate Injection, USP 20 mg/5 mL (4 mg/mL) multiple-dose vial by Amneal Pharmaceuticals LLC. The injection is for intramuscular or intravenous use and is prescription only. The label includes active ingredient details, storage instructions, manufacturer, and distributor information, and a barcode.*
FDA Label Image

4 (Dexamethasone Sodium Phosphate Injection Usp 4 mg 5)

4 (Dexamethasone Sodium Phosphate Injection Usp 4 mg  5)
Packaging label for Dexamethasone Sodium Phosphate Injection, USP 20 mg/5 mL (4 mg/mL) by Amneal Pharmaceuticals LLC. The label states the dosage form as injection solution, for intravenous, intramuscular, intra-articular, soft tissue, or intralesional use. It includes storage instructions, manufacturer information, and indicates 25 multiple-dose vials of 5 mL each.*
FDA Label Image

5 (Dexamethasone Sodium Phosphate Injection Usp 4 mg 6)

5 (Dexamethasone Sodium Phosphate Injection Usp 4 mg  6)
Label for Dexamethasone Sodium Phosphate Injection USP 4 mg/mL (120 mg/30 mL) by Amneal Pharmaceuticals LLC. The 30 mL multiple-dose vial is intended for intravenous, intramuscular, intra-articular, soft tissue, or intralesional use. Includes storage instructions, manufacturing and distribution details, and barcode.*
FDA Label Image

6 (Dexamethasone Sodium Phosphate Injection Usp 4 mg 7)

6 (Dexamethasone Sodium Phosphate Injection Usp 4 mg  7)
Label for Dexamethasone Sodium Phosphate Injection, USP 120 mg/30 mL (4 mg/mL) multiple dose vial. The label indicates intravenous, intramuscular, intra-articular, soft tissue, or intralesional use. Manufactured by Amneal Pharmaceuticals Pvt. Ltd. in India and distributed by Amneal Pharmaceuticals LLC, USA. Includes ingredients, 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.