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  5. NDC Package Code: 54458-300-31 Metoprolol Succinate

NDC Package 54458-300-31 Metoprolol Succinate

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:
54458-300-31
Package Description:
180 BLISTER PACK in 1 CARTON / 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (54458-300-30)
Product Code:
54458-300
Proprietary Name:
Metoprolol Succinate
Usage Information:
This medication is a beta-blocker used to treat chest pain (angina), heart failure, and high blood pressure. Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. This drug works by blocking the action of certain natural chemicals in your body (such as epinephrine) that affect the heart and blood vessels. This lowers heart rate, blood pressure, and strain on the heart.
11-Digit NDC Billing Format:
54458030031
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
180 EA
Labeler Name:
International Laboratories, Inc.
Sample Package:
No
FDA Application Number:
ANDA090615
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
09-22-2011
End Marketing Date:
06-06-2016
Listing Expiration Date:
06-06-2016
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 54458-300-31?

The NDC Packaged Code 54458-300-31 is assigned to a package of 180 blister pack in 1 carton / 30 tablet, film coated, extended release in 1 blister pack (54458-300-30) of Metoprolol Succinate, labeled by International Laboratories, Inc.. The product's dosage form is and is administered via form.

Is NDC 54458-300 included in the NDC Directory?

No, Metoprolol Succinate with product code 54458-300 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by International Laboratories, Inc. on September 22, 2011 and its listing in the NDC Directory is set to expire on June 06, 2016 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 54458-300-31?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 180.

What is the 11-digit format for NDC 54458-300-31?

The 11-digit format is 54458030031. 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
5-3-254458-300-315-4-254458-0300-31