Solu-medrol Injection, Powder, For Solution
Product Images NDC 84549-047

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Solu-medrol (NDC 84549-047). 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 047 22 Label)

This is a description of Solu-Medrol (PF) AOV 125mg/mL Injection USP that comes in a 2mL single dose vial for intravenous or intramuscular administration. The product should be protected from light and formulations with benzyl alcohol are not suitable for neonates. The unreconstituted product should be stored at room temperature, while the reconstituted solution needs to be used within 48 hours. The manufacturer information includes details like the lot number, expiration date, and item number. This prescription medication is produced by Pharmacia & Upjohn Company LLC and distributed by ProPharma Distribution LLC.*

FDA Label Image

Chemical Structure (Solu Medrol 01)

FDA Label Image

Figure (Solu Medrol 02)

FDA Label Image

Logo (Solu Medrol 03)

This text mentions a hospital product, "Q-P zer", which is distributed by Pharmacia & Upjohn Company LLC, a subsidiary of Pfizer Inc. This suggests that the product is related to healthcare and medical services. The location provided is New York, NY 10001.*

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