NDC Package 0469-2601-07 Myrbetriq

Mirabegron Tablet, Film Coated, Extended Release Oral - View Billable Units, 11-Digit Format, RxNorm

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:
0469-2601-07
Package Description:
4 CARTON in 1 TRAY / 1 BLISTER PACK in 1 CARTON / 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product Code:
Proprietary Name:
Myrbetriq
Non-Proprietary Name:
Mirabegron
Substance Name:
Mirabegron
Usage Information:
This medication is used to treat overactive bladder. Overactive bladder is a problem with how your bladder stores urine that causes a sudden urge to urinate. The urge may be hard to control, and overactive bladder symptoms may include frequent urination, strong sudden urges to urinate, or involuntary loss of urine (incontinence). Mirabegron works by relaxing a certain bladder muscle (detrusor), which helps the bladder hold more urine and lessens symptoms of overactive bladder.
11-Digit NDC Billing Format:
00469260107
NDC to RxNorm Crosswalk:
  • RxCUI: 1300791 - mirabegron 25 MG 24HR Extended Release Oral Tablet
  • RxCUI: 1300791 - 24 HR mirabegron 25 MG Extended Release Oral Tablet
  • RxCUI: 1300791 - mirabegron 25 MG 24 HR Release Tablet
  • RxCUI: 1300797 - Myrbetriq 25 MG 24HR Extended Release Oral Tablet
  • RxCUI: 1300797 - 24 HR mirabegron 25 MG Extended Release Oral Tablet [Myrbetriq]
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Astellas Pharma Us, Inc.
    Dosage Form:
    Tablet, Film Coated, Extended Release - 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; the tablet is formulated in such manner as to make the contained medicament available over an extended period of time following ingestion.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    Yes
    FDA Application Number:
    NDA202611
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    06-28-2012
    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
    0469-2601-301 BOTTLE in 1 CARTON / 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
    0469-2601-901 BOTTLE in 1 CARTON / 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0469-2601-07?

    The NDC Packaged Code 0469-2601-07 is assigned to a package of 4 carton in 1 tray / 1 blister pack in 1 carton / 7 tablet, film coated, extended release in 1 blister pack of Myrbetriq, a human prescription drug labeled by Astellas Pharma Us, Inc.. The product's dosage form is tablet, film coated, extended release and is administered via oral form.

    Is NDC 0469-2601 included in the NDC Directory?

    Yes, Myrbetriq with product code 0469-2601 is active and included in the NDC Directory. The product was first marketed by Astellas Pharma Us, Inc. on June 28, 2012 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 0469-2601-07?

    The 11-digit format is 00469260107. 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 4-4-2 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
    4-4-20469-2601-075-4-200469-2601-07