Solu-medrol Injection, Powder, For Solution
Product Images NDC 84549-039

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Solu-medrol (NDC 84549-039). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Propharma Distribution, 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

Label (84549 039 28)

Label (84549 039 28)
This is information about Solu-Medrol 40mg Injection USP in a 1mL multi-dose vial for intramuscular or intravenous use. The package does not contain a diluent, and a recommended diluent is Bacteriostatic Water for Injection containing Benzyl Alcohol as a preservative. The product should be stored at a controlled room temperature of 20 to 25 degrees Celsius. Once reconstituted, the solution should also be kept at the same temperature and used within 48 hours. Manufacturer information includes Pharmacia & Upjohn Company LLC. The lot number, expiration date, and packaging details are also provided.*
FDA Label Image

Chemical Structure (Solu Medrol 01)

FDA Label Image

Figure (Solu Medrol 02)

FDA Label Image

Logo (Solu Medrol 03)

Logo (Solu Medrol 03)
This is a description of a pharmaceutical product called Q-P zer, distributed by Pharmacia & Upjohn Company LLC, a subsidiary of Pfizer Inc. It is based in New York, NY 10001.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.