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

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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)
This is a description of a drug called Solu-Medrol (methylprednisolone sodium succinate) for injection. It comes in a 500 mg per vial dosage and is for intravenous or intramuscular use. It is preservative-free and comes with directions for use. After mixing, it should be stored at room temperature and used within 48 hours. The text also mentions the accompanying prescribing information and how to use the Act-0-Vial system. The text includes some references to product codes and distribution information from the Pharmacia & Upjohn Co division of Pfizer Inc.*
FDA Label Image

Description (Description)

Description (Description)
These are prescription medications containing methylprednisolone sodium succinate, used to treat conditions such as arthritis, blood disorders, severe allergic reactions, certain cancers and weakening of the immune system. The formulations come in various strengths and some are free from preservatives, while others contain benzyl alcohol as a preservative. Diluent, which may contain benzyl alcohol, is required to reconstitute the medication and should be used within 48 hours after mixing.*
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Dosage (Dosage 1)

Dosage (Dosage 1)
This text appears to be a list of different types of corticosteroids and their respective dosages. It could potentially be used for medical or pharmaceutical purposes.*
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Dosage I (Dosage Image)

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How Supplied 1 (How Supplied 1)

How Supplied 1 (How Supplied 1)
This text provides information on different drugs and their packaging. The first two listings show two vials, one containing 500 mg and the other containing 1 gram of medication in a multi-dose vial format, each with a different volume of 8 mL and 16 mL, respectively, and both with the National Drug Code (NDC) 0009-0758-01 and 0009-0698-01. The last listing shows a 2-gram vial of medication that comes with a diluent solution, with an NDC code of 0009-0796-01.*
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How Supplied 2 (How Supplied 2)

How Supplied 2 (How Supplied 2)
This is a list of Act-O-Vial System presentations with their respective sizes and National Drug Codes (NDC). The Act-O-Vial System comes in different doses and volumes, ranging from 40mg in a 1mL single-use vial to 1g in an 8mL single-use vial. These descriptions are commonly used in the pharmaceutical industry to identify and differentiate different product presentations.*
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Logo (Logo)
G tectabies is a product distributed by Pharmacia & Upjohn Co, a division of Pfizer Inc located in New York, NY 10017.*
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Serialized Carton Labeling (Serialized Labeling R)

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Structure (Structure)

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Vial Label (Vial Label)

Vial Label (Vial Label)
This is a description of a medication called "methylprednisolone sodium succinate for injection, USP". It is meant for intramuscular or intravenous use and comes in a single-use vial with an NDC number. The solution should be stored at a controlled room temperature of 20 to 25°C and used within 48 hours of mixing. Once reconstituted with 4 mL of the Diluent, the concentration is 125 mg per mL. The medication is distributed by Pharmacia & Upjohn Co as a prescription-only drug and is preservative-free.*

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