NDC Package 67046-1109-3 Metoprolol Succinate

Metoprolol Succinate Er Tablets Tablet, Film Coated, Extended Release Oral - View Billable Units, 11-Digit Format, RxNorm

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:
67046-1109-3
Package Description:
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product Code:
Proprietary Name:
Metoprolol Succinate
Non-Proprietary Name:
Metoprolol Succinate Er Tablets
Substance 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:
67046110903
NDC to RxNorm Crosswalk:
  • RxCUI: 866412 - metoprolol succinate 100 MG 24HR Extended Release Oral Tablet
  • RxCUI: 866412 - 24 HR metoprolol succinate 100 MG Extended Release Oral Tablet
  • RxCUI: 866412 - 24 HR metoprolol succinate 100 MG (as metoprolol succinate 95 MG equivalent to 100 MG metoprolol tartrate) Extended Release Oral Tablet
  • RxCUI: 866412 - metoprolol succinate 100 MG 24 HR Extended Release Oral Tablet
Product Type:
Human Prescription Drug
Labeler Name:
Coupler Llc
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(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Sample Package:
No
FDA Application Number:
ANDA211143
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
11-12-2024
Listing Expiration Date:
12-31-2025
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.

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Frequently Asked Questions

What is NDC 67046-1109-3?

The NDC Packaged Code 67046-1109-3 is assigned to a package of 30 tablet, film coated, extended release in 1 blister pack of Metoprolol Succinate, a human prescription drug labeled by Coupler Llc. The product's dosage form is tablet, film coated, extended release and is administered via oral form.

Is NDC 67046-1109 included in the NDC Directory?

Yes, Metoprolol Succinate with product code 67046-1109 is active and included in the NDC Directory. The product was first marketed by Coupler Llc on November 12, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 67046-1109-3?

The 11-digit format is 67046110903. 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
5-4-167046-1109-35-4-267046-1109-03