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  5. NDC Package Code: 71269-040-10 Tuxarin

NDC Package 71269-040-10 Tuxarin

Codeine Phosphate And Chlorpheniramine Maleate 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:
71269-040-10
Package Description:
100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Code:
71269-040
Proprietary Name:
Tuxarin
Non-Proprietary Name:
Codeine Phosphate And Chlorpheniramine Maleate
Substance Name:
Chlorpheniramine Maleate; Codeine Phosphate
Usage Information:
TUXARIN ER is indicated for the relief of cough and symptoms associated with upper respiratory allergies or a common cold in adults 18 years of age and older.
11-Digit NDC Billing Format:
71269004010
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
100 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1664543 - codeine phosphate 54.3 MG / chlorpheniramine maleate 8 MG 12HR Oral Extended Release Tablet
  • RxCUI: 1664543 - 12 HR chlorpheniramine maleate 8 MG / codeine phosphate 54.3 MG Extended Release Oral Tablet
  • RxCUI: 1664543 - chlorpheniramine maleate 8 MG / codeine phosphate 54.3 MG 12HR Oral Extended Release Tablet
  • RxCUI: 2099286 - Tuxarin ER 54.3 MG / 8 MG 12HR Extended Release Oral Tablet
  • RxCUI: 2099286 - 12 HR chlorpheniramine maleate 8 MG / codeine phosphate 54.3 MG Extended Release Oral Tablet [Tuxarin]
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Mainpointe Pharmaceuticals
    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):
  • CHLORPHENIRAMINE MALEATE 8 mg/1
  • CODEINE PHOSPHATE 54.3 mg/1
    • Pharmacologic Class(es):
  • Full Opioid Agonists - [MoA] (Mechanism of Action)
  • Histamine H1 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Histamine-1 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
  • Opioid Agonist - [EPC] (Established Pharmacologic Class)
    • DEA Schedule:
    Schedule III (CIII) Substances
    Sample Package:
    No
    FDA Application Number:
    NDA206323
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    10-15-2018
    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
    71269-040-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 71269-040-10?

    The NDC Packaged Code 71269-040-10 is assigned to a package of 100 tablet, extended release in 1 bottle, plastic of Tuxarin, a human prescription drug labeled by Mainpointe Pharmaceuticals. The product's dosage form is tablet, extended release and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 100 billable units per package.

    Is NDC 71269-040 included in the NDC Directory?

    Yes, Tuxarin with product code 71269-040 is active and included in the NDC Directory. The product was first marketed by Mainpointe Pharmaceuticals on October 15, 2018 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 NDC billing unit for package 71269-040-10?

    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 100.

    What is the 11-digit format for NDC 71269-040-10?

    The 11-digit format is 71269004010. 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
    5-3-271269-040-105-4-271269-0040-10