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  5. NDC Package Code: 67046-1569-3 Metoprolol Tartrate

NDC Package 67046-1569-3 Metoprolol Tartrate

Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

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:
67046-1569-3
Package Description:
30 TABLET in 1 BLISTER PACK
Product Code:
67046-1569
Proprietary Name:
Metoprolol Tartrate
Non-Proprietary Name:
Metoprolol Tartrate
Substance Name:
Metoprolol Tartrate
Usage Information:
Metoprolol is used with or without other medications to treat high blood pressure (hypertension). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. This medication is also used to treat chest pain (angina) and to improve survival after a heart attack. Metoprolol belongs to a class of drugs known as beta blockers. It works by blocking the action of certain natural chemicals in your body, such as epinephrine, on the heart and blood vessels. This effect lowers the heart rate, blood pressure, and strain on the heart.
11-Digit NDC Billing Format:
67046156903
Product Type:
Human Prescription Drug
Labeler Name:
Coupler Llc
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
METOPROLOL TARTRATE 50 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA200981
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
06-17-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
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 67046-1569-3?

The NDC Packaged Code 67046-1569-3 is assigned to a package of 30 tablet in 1 blister pack of Metoprolol Tartrate, a human prescription drug labeled by Coupler Llc. The product's dosage form is tablet and is administered via oral form.

Is NDC 67046-1569 included in the NDC Directory?

Yes, Metoprolol Tartrate with product code 67046-1569 is active and included in the NDC Directory. The product was first marketed by Coupler Llc on June 17, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 67046-1569-3?

The 11-digit format is 67046156903. 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
5-4-167046-1569-35-4-267046-1569-03