NDC Package 58118-0734-8 Metoprolol Succinate

View Billable Units, 11-Digit Format, RxNorm

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:
58118-0734-8
Package Description:
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product Code:
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:
58118073408
Labeler Name:
Clinical Solutions Wholesale
Sample Package:
No
FDA Application Number:
ANDA090615
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
07-22-2010
End Marketing Date:
06-15-2017
Listing Expiration Date:
06-15-2017
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
58118-0734-01 TABLET, FILM COATED, EXTENDED RELEASE in 1 PACKET
58118-0734-330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
58118-0734-660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
58118-0734-990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 58118-0734-8?

The NDC Packaged Code 58118-0734-8 is assigned to a package of 30 tablet, film coated, extended release in 1 blister pack of Metoprolol Succinate, labeled by Clinical Solutions Wholesale. The product's dosage form is and is administered via form.

Is NDC 58118-0734 included in the NDC Directory?

The product was first marketed by Clinical Solutions Wholesale on July 22, 2010 and its listing in the NDC Directory is set to expire on June 15, 2017 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 58118-0734-8?

The 11-digit format is 58118073408. 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
5-4-158118-0734-85-4-258118-0734-08