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  5. NDC Package Code: 68071-1792-2 Solu-medrol

NDC Package 68071-1792-2 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 because the listing data was inactivated by the FDA.

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:
68071-1792-2
Package Description:
2 mL in 1 BOTTLE, GLASS
Product Code:
68071-1792
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:
68071179202
NDC to RxNorm Crosswalk:
  • RxCUI: 1743704 - methylPREDNISolone sodium succinate 125 MG Injection
  • RxCUI: 1743704 - methylprednisolone 125 MG Injection
  • RxCUI: 1743704 - methylprednisolone (as methylprednisolone sodium succinate) 125 MG Injection
  • RxCUI: 1743707 - SOLU-Medrol 125 MG Injection
  • RxCUI: 1743707 - methylprednisolone 125 MG Injection [Solu-Medrol]
    • Labeler Name:
    Nucare Pharmaceuticals,inc.
    Sample Package:
    No
    Start Marketing Date:
    04-02-1959
    Listing Expiration Date:
    12-31-2022
    Exclude Flag:
    I
    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 68071-1792-2?

    The NDC Packaged Code 68071-1792-2 is assigned to a package of 2 ml in 1 bottle, glass of Solu-medrol, labeled by Nucare Pharmaceuticals,inc.. The product's dosage form is and is administered via form.

    Is NDC 68071-1792 included in the NDC Directory?

    No, Solu-medrol with product code 68071-1792 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Nucare Pharmaceuticals,inc. on April 02, 1959 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 68071-1792-2?

    The 11-digit format is 68071179202. 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 5-4-1 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
    5-4-168071-1792-25-4-268071-1792-02