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  5. NDC Package Code: 55111-469-78 Metoprolol Succinate

NDC Package 55111-469-78 Metoprolol Succinate

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

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
55111-469-78
Package Description:
10 BLISTER PACK in 1 CARTON / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (55111-469-79)
Product Code:
55111-469
Proprietary Name:
Metoprolol Succinate
Non-Proprietary Name:
Metoprolol Succinate
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:
55111046978
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
  • RxCUI: 866419 - metoprolol succinate 200 MG 24HR Extended Release Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Dr. Reddy's Laboratories Limited
    Dosage Form:
    Tablet, Extended Release - A solid dosage form containing a drug which allows at least a reduction in dosing frequency as compared to that drug presented in conventional dosage form.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • METOPROLOL SUCCINATE 200 mg/1
    • Pharmacologic Class(es):
  • Adrenergic beta-Antagonists - [MoA] (Mechanism of Action)
  • beta-Adrenergic Blocker - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA078889
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    09-10-2012
    Listing Expiration Date:
    12-31-2024
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    55111-469-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE
    55111-469-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE
    55111-469-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE
    55111-469-6060 TABLET, EXTENDED RELEASE in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 55111-469-78?

    The NDC Packaged Code 55111-469-78 is assigned to a package of 10 blister pack in 1 carton / 10 tablet, extended release in 1 blister pack (55111-469-79) of Metoprolol Succinate, a human prescription drug labeled by Dr. Reddy's Laboratories Limited. The product's dosage form is tablet, extended release and is administered via oral form.

    Is NDC 55111-469 included in the NDC Directory?

    Yes, Metoprolol Succinate with product code 55111-469 is active and included in the NDC Directory. The product was first marketed by Dr. Reddy's Laboratories Limited on September 10, 2012 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 55111-469-78?

    The 11-digit format is 55111046978. 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
    5-3-255111-469-785-4-255111-0469-78