Figure 1 (Methylprednisolone Acetate Injectable Suspension U 1)
Methylprednisolone Acetate Injection, Suspension
Product Images NDC 42023-239
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Product Visual Gallery
This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Methylprednisolone Acetate (NDC 42023-239). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Endo Usa, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
400 mg/5 mL Carton (Methylprednisolone Acetate Injectable Suspension U 2)
MethylPREDNISolone Acetate Injectable Suspension, USP is a multi-dose vial containing 400 mg/5 mL (80 mg/mL) methylprednisolone acetate. It is for intramuscular, intrasynovial and soft tissue injection only and must not be used intravenously. This drug is not available to the general public and requires a prescription. It contains benzyl alcohol as a preservative and must be stored between 20° to 25°C (66° to 77°F). The vial stopper is not made with natural rubber latex. Dosage instructions can be found in the full prescribing information. The text also includes information about the manufacturer, Par Pharmaceutical, location in Chestnut Ridge, NY 10977, and the NDC number, 42023-240-01.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
