Metoprolol Succinate Tablet, Film Coated, Extended Release
NDC Package 72162-1859-0

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Metoprolol Succinate (metoprolol succinate er tablets) tablets is a medication a beta-blocker used to treat chest pain (angina), heart failure, and high blood pressure. This formulation utilizes a tablet, film coated, extended release delivery system. Marketed by Bryant Ranch Prepack, this product is identified by NDC 72162-1859 and is authorized under FDA application ANDA211143.

Identification & Billing

NDC Package Code
72162-1859-0
Package Description
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Code
72162-1859
11-Digit Billing Format
72162185900
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
1000 EA
RxNorm Crosswalk
  • RxCUI: 866419 - metoprolol succinate 200 MG 24HR Extended Release Oral Tablet
  • RxCUI: 866419 - 24 HR metoprolol succinate 200 MG Extended Release Oral Tablet
  • RxCUI: 866419 - 24 HR metoprolol succinate 200 MG (as metoprolol succinate 190 MG equivalent to 200 MG metoprolol tartrate) Extended Release Oral Tablet
  • RxCUI: 866419 - metoprolol succinate 200 MG 24 HR Extended Release Oral Tablet

Clinical Specifications

Proprietary Name
Metoprolol Succinate
Non-Proprietary Name
Metoprolol Succinate Er Tablets
Substance Name
Metoprolol Succinate
Dosage Form
Tablet, Film Coated, Extended Release - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer; the tablet is formulated in such manner as to make the contained medicament available over an extended period of time following ingestion.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
METOPROLOL SUCCINATE 200 mg/1
Pharmacologic Class
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.

Regulatory & Marketing

Labeler Name
Bryant Ranch Prepack
Product Type
Human Prescription Drug
FDA Application #
ANDA211143
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
11-27-2020
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (72162-1859). Click a package code to view its specific billing and regulatory data.

72162-1859-1
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
72162-1859-5
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 72162-1859-0 identifies a specific commercial package of 1000 tablet, film coated, extended release in 1 bottle of Metoprolol Succinate, a human prescription drug labeled by Bryant Ranch Prepack. This product is billed for "EA" each discreet unit and contains an estimated amount of 1000 billable units per package. This tablet, film coated, extended release is formulated for oral use and contains metoprolol succinate as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Bryant Ranch Prepack on November 27, 2020. The current certification is valid through December 31, 2026.

What are the primary indications for this medication?

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.

How is this Bryant Ranch Prepack product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72162185900. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 1000 total billable units per package. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
72162-1859-0
11-Digit CMS (5-4-2)
72162-1859-00

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.