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  5. NDC Package Code: 64842-1020-1 Lonsurf

NDC Package 64842-1020-1 Lonsurf

Trifluridine And Tipiracil 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:
64842-1020-1
Package Description:
20 TABLET, FILM COATED in 1 BOTTLE
Product Code:
64842-1020
Proprietary Name:
Lonsurf
Non-Proprietary Name:
Trifluridine And Tipiracil
Substance Name:
Tipiracil Hydrochloride; Trifluridine
Usage Information:
This medication is used to treat certain cancers (such as stomach, colon/rectum). It works by slowing or stopping the growth of cancer cells.
11-Digit NDC Billing Format:
64842102001
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
20 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1670311 - tipiracil 6.14 MG / trifluridine 15 MG Oral Tablet
  • RxCUI: 1670316 - tipiracil 8.19 MG / trifluridine 20 MG Oral Tablet
  • RxCUI: 1670322 - Lonsurf 15 MG / 6.14 MG Oral Tablet
  • RxCUI: 1670322 - tipiracil 6.14 MG / trifluridine 15 MG Oral Tablet [Lonsurf]
  • RxCUI: 1670322 - Lonsurf (trifluridine 15 MG / tipiracil 6.14 MG) Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Taiho Pharmaceutical Co., Ltd.
    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):
  • TIPIRACIL HYDROCHLORIDE 8.19 mg/1
  • TRIFLURIDINE 20 mg/1
    • Pharmacologic Class(es):
  • Nucleic Acid Synthesis Inhibitors - [MoA] (Mechanism of Action)
  • Nucleoside Analog Antiviral - [EPC] (Established Pharmacologic Class)
  • Nucleoside Analog - [EXT]
  • Nucleoside Metabolic Inhibitor - [EPC] (Established Pharmacologic Class)
  • Thymidine Phosphorylase Inhibitor - [EPC] (Established Pharmacologic Class)
  • Thymidine Phosphorylase Inhibitors - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    NDA207981
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    09-22-2015
    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
    64842-1020-240 TABLET, FILM COATED in 1 BOTTLE
    64842-1020-360 TABLET, FILM COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 64842-1020-1?

    The NDC Packaged Code 64842-1020-1 is assigned to a package of 20 tablet, film coated in 1 bottle of Lonsurf, a human prescription drug labeled by Taiho Pharmaceutical Co., Ltd.. The product's dosage form is tablet, film coated and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 20 billable units per package.

    Is NDC 64842-1020 included in the NDC Directory?

    Yes, Lonsurf with product code 64842-1020 is active and included in the NDC Directory. The product was first marketed by Taiho Pharmaceutical Co., Ltd. on September 22, 2015 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 NDC billing unit for package 64842-1020-1?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 20.

    What is the 11-digit format for NDC 64842-1020-1?

    The 11-digit format is 64842102001. 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
    5-4-164842-1020-15-4-264842-1020-01