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  5. NDC Package Code: 53489-461-01 Quinidine Sulfate

NDC Package 53489-461-01 Quinidine Sulfate

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
53489-461-01
Package Description:
100 TABLET in 1 BOTTLE, PLASTIC
Product Code:
53489-461
Proprietary Name:
Quinidine Sulfate
Usage Information:
This medication is used to treat or prevent many types of irregular heartbeats (heart arrhythmias such as atrial fibrillation). Quinidine can greatly improve your ability to perform normal activities by decreasing the number of irregular heartbeats you have. However, it may not stop all your irregular heartbeats completely. It works by blocking abnormal heartbeat signals. Before and while you are using quinidine, your doctor may prescribe other medications (e.g., "blood thinners"/anticoagulants such as warfarin, beta blockers such as metoprolol) to shrink any blood clots in the heart and to slow your pulse.
11-Digit NDC Billing Format:
53489046101
Labeler Name:
Mutual Pharmaceutical Company, Inc.
Sample Package:
No
FDA Application Number:
ANDA081030
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
04-14-1989
End Marketing Date:
02-29-2012
Listing Expiration Date:
02-29-2012
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
53489-461-0250 TABLET in 1 BOTTLE, PLASTIC
53489-461-03250 TABLET in 1 BOTTLE, PLASTIC
53489-461-05500 TABLET in 1 BOTTLE, PLASTIC
53489-461-101000 TABLET in 1 BOTTLE, PLASTIC

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 53489-461-01?

The NDC Packaged Code 53489-461-01 is assigned to a package of 100 tablet in 1 bottle, plastic of Quinidine Sulfate, labeled by Mutual Pharmaceutical Company, Inc.. The product's dosage form is and is administered via form.

Is NDC 53489-461 included in the NDC Directory?

No, Quinidine Sulfate with product code 53489-461 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Mutual Pharmaceutical Company, Inc. on April 14, 1989 and its listing in the NDC Directory is set to expire on February 29, 2012 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 53489-461-01?

The 11-digit format is 53489046101. 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
5-3-253489-461-015-4-253489-0461-01