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  5. NDC Package Code: 70518-2914-0 Methylprednisolone Acetate

NDC Package 70518-2914-0 Methylprednisolone Acetate

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 discontinued by the firm.

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:
70518-2914-0
Package Description:
1 VIAL, MULTI-DOSE in 1 CARTON / 10 mL in 1 VIAL, MULTI-DOSE
Product Code:
70518-2914
Proprietary Name:
Methylprednisolone Acetate
Usage Information:
Methylprednisolone is used to treat pain and swelling that occurs with arthritis and other joint disorders. This medication may also be used to treat various conditions such as blood disorders, severe allergic reactions, certain cancers, eye conditions, skin/intestinal/kidney/lung diseases, and immune system disorders. It decreases your immune system's response to these conditions and reduces symptoms such as swelling, pain, and allergic-type reactions. 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 is a corticosteroid hormone. Methylprednisolone may also be used with other medications in hormone disorders.
11-Digit NDC Billing Format:
70518291400
Labeler Name:
Remedyrepack Inc.
Sample Package:
No
FDA Application Number:
ANDA040620
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
10-21-2020
End Marketing Date:
10-21-2020
Listing Expiration Date:
10-21-2020
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 70518-2914-0?

The NDC Packaged Code 70518-2914-0 is assigned to a package of 1 vial, multi-dose in 1 carton / 10 ml in 1 vial, multi-dose of Methylprednisolone Acetate, labeled by Remedyrepack Inc.. The product's dosage form is and is administered via form.

Is NDC 70518-2914 included in the NDC Directory?

No, Methylprednisolone Acetate with product code 70518-2914 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Remedyrepack Inc. on October 21, 2020 and its listing in the NDC Directory is set to expire on October 21, 2020 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 70518-2914-0?

The 11-digit format is 70518291400. 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
5-4-170518-2914-05-4-270518-2914-00