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  5. NDC Package Code: 53489-551-07 Propafenone Hydrochloride

NDC Package 53489-551-07 Propafenone Hydrochloride

Tablet, Film Coated 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:
53489-551-07
Package Description:
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Code:
53489-551
Proprietary Name:
Propafenone Hydrochloride
Non-Proprietary Name:
Propafenone Hydrochloride
Substance Name:
Propafenone Hydrochloride
Usage Information:
Propafenone hydrochloride tablets are indicated to:•prolong the time to recurrence of paroxysmal atrial fibrillation/flutter (PAF) associated with disabling symptoms in patients without structural heart disease.•prolong the time to recurrence of paroxysmal supraventricular tachycardia (PSVT) associated with disabling symptoms in patients without structural heart disease.•treat documented ventricular arrhythmias, such as sustained ventricular tachycardia that, in the judgment of the physician, are life-threatening. Initiate treatment in the hospital.
11-Digit NDC Billing Format:
53489055107
NDC to RxNorm Crosswalk:
  • RxCUI: 861424 - propafenone HCl 150 MG Oral Tablet
  • RxCUI: 861424 - propafenone hydrochloride 150 MG Oral Tablet
  • RxCUI: 861427 - propafenone HCl 225 MG Oral Tablet
  • RxCUI: 861427 - propafenone hydrochloride 225 MG Oral Tablet
  • RxCUI: 861430 - propafenone HCl 300 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Sun Pharmaceutical Industries, Inc.
    Dosage Form:
    Tablet, Film Coated - 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.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • PROPAFENONE HYDROCHLORIDE 150 mg/1
    • Pharmacologic Class(es):
  • Antiarrhythmic - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA075998
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-29-2001
    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
    53489-551-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    53489-551-03250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    53489-551-05500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    53489-551-101000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 53489-551-07?

    The NDC Packaged Code 53489-551-07 is assigned to a package of 30 tablet, film coated in 1 bottle, plastic of Propafenone Hydrochloride, a human prescription drug labeled by Sun Pharmaceutical Industries, Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 53489-551 included in the NDC Directory?

    Yes, Propafenone Hydrochloride with product code 53489-551 is active and included in the NDC Directory. The product was first marketed by Sun Pharmaceutical Industries, Inc. on November 29, 2001 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 53489-551-07?

    The 11-digit format is 53489055107. 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
    5-3-253489-551-075-4-253489-0551-07