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  5. NDC Package Code: 52125-144-01 Solu-medrol

NDC Package 52125-144-01 Solu-medrol

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory .

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
52125-144-01
Package Description:
1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product Code:
52125-144
Proprietary Name:
Solu-medrol
Usage Information:
This medication is used to treat conditions such as arthritis, blood disorders, severe allergic reactions, certain cancers, eye conditions, skin/kidney/intestinal/lung diseases, and immune system disorders. It decreases your immune system's response to various diseases to reduce symptoms such as swelling, pain, and allergic-type reactions. Methylprednisolone is a corticosteroid hormone. This injectable form of methylprednisolone is used when a similar drug cannot be taken by mouth or when a very fast response is needed, especially in patients with severe medical conditions. Talk to your doctor about the risks and benefits of methylprednisolone, especially if it is to be injected near your spine (epidural). Rare but serious side effects may occur with epidural use. Methylprednisolone may also be used with other medications in hormone disorders.
11-Digit NDC Billing Format:
52125014401
Labeler Name:
Remedyrepack Inc.
Sample Package:
No
FDA Application Number:
NDA011856
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
07-18-2012
End Marketing Date:
05-27-2015
Listing Expiration Date:
05-27-2015
Exclude Flag:
D
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 52125-144-01?

The NDC Packaged Code 52125-144-01 is assigned to a package of 1 injection, powder, for solution in 1 vial of Solu-medrol, labeled by Remedyrepack Inc.. The product's dosage form is and is administered via form.

Is NDC 52125-144 included in the NDC Directory?

The product was first marketed by Remedyrepack Inc. on July 18, 2012 and its listing in the NDC Directory is set to expire on May 27, 2015 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 52125-144-01?

The 11-digit format is 52125014401. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-252125-144-015-4-252125-0144-01