Solu-medrol(r) Methylprednisolone Sodium Succinat Injection, Powder, For Solution
Product Images NDC 51662-1483

10 FDA label images from Hf Acquisition Co Llc, Dba Healthfirst · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Solu-medrol(r) Methylprednisolone Sodium Succinat (NDC 51662-1483). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Carton Label (Carton Label)

Carton Label (Carton Label)
Packaging label for Solu-Medrol (methylprednisolone sodium succinate) injection, powder for solution, 500 mg per vial. The label indicates use for intramuscular or intravenous administration and states it is preservative-free. The label also lists storage instructions, dosage preparation directions, and Pfizer branding with the note 'Rx only.'*
FDA Label Image

Description (Description)

Description (Description)
Text panel listing preservative-free and benzyl alcohol-preserved formulations of methylprednisolone sodium succinate injection in various strengths and vial sizes, including 40 mg, 125 mg, 500 mg, 1 gram, and 2 gram Act-O-Vial systems. It provides details on content per mL or vial once mixed, mentions recommended diluents, and highlights the importance of using only the accompanying diluent and using the product within 48 hours after mixing.*
FDA Label Image

Dosage (Dosage 1)

Dosage (Dosage 1)
A data table listing corticosteroids with their respective potencies. It includes Cortisone (25), Hydrocortisone (20), Prednisolone (5), Prednisone (5), Methylprednisolone (4), Triamcinolone (4), Paramethasone (2), Betamethasone (0.75), and Dexamethasone (0.75).*
FDA Label Image

Dosage I (Dosage Image)

Dosage I (Dosage Image)
An illustrative diagram showing a cross-sectional view of a vial stopper and a syringe needle puncturing it, demonstrating the mechanism of vial access for injection preparation.*
FDA Label Image

How Supplied 1 (How Supplied 1)

How Supplied 1 (How Supplied 1)
A table listing SOLU-MEDROL methylprednisolone sodium succinate vial sizes and NDC numbers, including 500 mg multi-dose vial (8 mL), 1 gram multi-dose vial (16 mL), and 2 gram vial with diluent. Each entry shows corresponding NDC codes.*
FDA Label Image

How Supplied 2 (How Supplied 2)

How Supplied 2 (How Supplied 2)
A data table listing packaging configurations for SOLU-MEDROL Methylprednisolone Sodium Succinat injection, powder for solution. It shows Act-O-Vial single-use vials in strengths of 40 mg (25 x 1 mL), 125 mg (25 x 2 mL), 500 mg (4 mL), and 1 gram (8 mL) with their respective National Drug Codes (NDCs).*
FDA Label Image
FDA Label Image

Serialized Carton Labeling (Serialized Labeling R)

Serialized Carton Labeling (Serialized Labeling R)
Packaging label for Solu-Medrol (methylprednisolone sodium succinate) injection powder, 500 mg per vial, for intramuscular or intravenous use. The single-use vial is preservative-free and contains 4 mL Act-O-Vial. The product is labeled for Rx only and distributed by Pharmacia & Upjohn Co, a division of Pfizer Inc.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of methylprednisolone sodium succinate, shown with labeled functional groups and rings characteristic of the corticosteroid molecule.*
FDA Label Image

Vial Label (Vial Label)

Vial Label (Vial Label)
Label for Solu-Medrol (methylprednisolone sodium succinate) injection powder for solution, 500 mg per vial. Designed for intramuscular or intravenous use, preservative-free, single-use vial with 4 mL Act-O-Vial. Distributed by Pharmacia & Upjohn Co, a division of Pfizer, NY.*

* 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.