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  5. NDC Package Code: 52125-836-57 Menactra

NDC Package 52125-836-57 Menactra

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:
52125-836-57
Package Description:
.5 mL in 1 VIAL, SINGLE-DOSE
Product Code:
52125-836
Proprietary Name:
Menactra
Usage Information:
This vaccine is used to help prevent certain serious, sometimes fatal, bacterial infections (meningitis, meningococcemia). This infection may cause severe problems (hearing loss, brain/nerve problems, paralysis, blindness, seizures, loss of limbs) even with antibiotic treatment. This vaccine works by increasing the body's natural defense (immunity) against the bacteria that cause meningococcal disease. Vaccination is the best way to prevent infection. However, like any vaccine, it may not fully protect everyone who receives it. The brand and dose of vaccine you receive depend on your age. Other vaccines may also be given at the same time, usually in a different site on the body.
11-Digit NDC Billing Format:
52125083657
Labeler Name:
Remedyrepack Inc.
Sample Package:
No
FDA Application Number:
BLA125089
Marketing Category:
BLA - A product marketed under an approved Biologic License Application.
Start Marketing Date:
01-03-2015
End Marketing Date:
03-29-2016
Listing Expiration Date:
03-29-2016
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 52125-836-57?

The NDC Packaged Code 52125-836-57 is assigned to a package of .5 ml in 1 vial, single-dose of Menactra, labeled by Remedyrepack Inc.. The product's dosage form is and is administered via form.

Is NDC 52125-836 included in the NDC Directory?

No, Menactra with product code 52125-836 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Remedyrepack Inc. on January 03, 2015 and its listing in the NDC Directory is set to expire on March 29, 2016 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 52125-836-57?

The 11-digit format is 52125083657. 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
5-3-252125-836-575-4-252125-0836-57