Dexamethasone Sodium Phosphate Injection, Solution
Product Images NDC 71872-7128

3 FDA label images from Medical Purchasing Solutions, 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 71872-7128). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, 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

Pdp (7128)

Pdp (7128)
Dexamethasone Sodium Phosphate Injection USP 20 mg per 5 mL (4 mg/mL) multiple-dose vial label. The label indicates a 5 mL vial with 4 mg/mL strength, for intravenous, intramuscular, intra-articular, soft tissue, or intralesional use. Distributed by Medical Purchasing Solutions, LLC, Scottsdale, AZ, and manufactured by AuroMedics Pharma LLC. The label includes storage instructions and ingredients, noting the product is made in India.*
FDA Label Image

Label (Dexamethasone Fig3)

Label (Dexamethasone Fig3)
Label for Dexamethasone Sodium Phosphate Injection USP, 4 mg/mL (20 mg per 5 mL), in a 5 mL multiple-dose vial. The label includes usage routes for intravenous or intramuscular use, storage instructions, preservative information, and manufacturer details listing AuroMedics Pharma LLC, E. Windsor, NJ.*
FDA Label Image

Dexamethasone Sodium Phosphate Chemical Structure (Dexamethasone Str)

Dexamethasone Sodium Phosphate Chemical Structure (Dexamethasone Str)
Chemical structure diagram of dexamethasone sodium phosphate, showing the molecular arrangement including phosphate groups and characteristic steroid rings.*

* 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.