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  5. NDC Package Code: 75929-098-12 Banzel

NDC Package 75929-098-12 Banzel

Rufinamide 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:
75929-098-12
Package Description:
120 TABLET, FILM COATED in 1 BOTTLE
Product Code:
75929-098
Proprietary Name:
Banzel
Non-Proprietary Name:
Rufinamide
Substance Name:
Rufinamide
Usage Information:
Rufinamide is used with other medications to prevent or control seizures (epilepsy) associated with Lennox-Gastaut syndrome (LGS). This medication is an anticonvulsant. Rufinamide is thought to work by acting on the sodium channels in the brain that carry excessive electrical charges that may cause seizures.
11-Digit NDC Billing Format:
75929009812
Product Type:
Human Prescription Drug
Labeler Name:
Pharma Packaging Solutions, Llc Dba Tjoapack Llc
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):
  • RUFINAMIDE 400 mg/1
    • Sample Package:
    No
    FDA Application Number:
    NDA021911
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    11-14-2008
    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.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    75929-098-51120 TABLET, FILM COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 75929-098-12?

    The NDC Packaged Code 75929-098-12 is assigned to a package of 120 tablet, film coated in 1 bottle of Banzel, a human prescription drug labeled by Pharma Packaging Solutions, Llc Dba Tjoapack Llc. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 75929-098 included in the NDC Directory?

    Yes, Banzel with product code 75929-098 is active and included in the NDC Directory. The product was first marketed by Pharma Packaging Solutions, Llc Dba Tjoapack Llc on November 14, 2008 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 75929-098-12?

    The 11-digit format is 75929009812. 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
    5-3-275929-098-125-4-275929-0098-12