Solu-medrol Injection, Powder, For Solution
Product Images NDC 71872-7232

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Solu-medrol (NDC 71872-7232). 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

71872-7232-1.pdp (71872 7232 1)

SOLU-MEDROL 125 mg/2 mL injection, powder, for solution vial label for methylprednisolone sodium succinate. The label indicates single-use vial containing 125 mg per 2 mL, with lot and expiration date placeholders. Instructions include storage at controlled room temperature and directions for reconstitution and use. Labeler and distributor is Medical Purchasing Solutions, LLC, Scottsdale, AZ.*

FDA Label Image

Chemical Structure (Solu Medrol 01)

Chemical structure of methylprednisolone sodium succinate, the active ingredient in SOLU-MEDROL 125 mg/2mL injection powder for solution, shown with hydroxyl, carbonyl, and carboxylate functional groups.*

FDA Label Image

Image (Solu Medrol 02)

Instructional diagram showing a medical syringe needle puncturing a vial septum, depicting the process of withdrawing medication from a sealed vial for injection.*

FDA Label Image

Logo (Solu Medrol 03)

FDA Label Image

Principal Display Panel (125 mg Vial Label)

Label for SOLU-MEDROL 125 mg per vial injection powder for solution, methylprednisolone sodium succinate, USP. It is a 2 mL Act-O-Vial single-dose vial for intramuscular or intravenous use, preservative-free. The label includes dosage and use instructions, storage directions, lot/expiration information, and notes it is distributed by Medical Purchasing Solutions, LLC.*

* 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.