NDC Package 21695-148-15 Actos

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
Package Description:
Product Code:
Proprietary Name:
Usage Information:
Pioglitazone is a diabetes drug (thiazolidinedione-type, also called "glitazones") used along with a proper diet and exercise program to control high blood sugar in patients with type 2 diabetes. It works by helping to restore your body's proper response to insulin, thereby lowering your blood sugar. Controlling high blood sugar helps prevent kidney damage, blindness, nerve problems, loss of limbs, and sexual function problems. Proper control of diabetes may also lessen your risk of a heart attack or stroke. Pioglitazone is used either alone or in combination with other diabetes medications (such as metformin or a sulfonylurea such as glyburide). Talk to your doctor about the risks and benefits of pioglitazone.
11-Digit NDC Billing Format:
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
15 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 261266 - Actos 15 MG Oral Tablet
  • RxCUI: 261266 - pioglitazone 15 MG Oral Tablet [Actos]
  • RxCUI: 261266 - Actos (as pioglitazone hydrochloride) 15 MG Oral Tablet
  • RxCUI: 261267 - Actos 30 MG Oral Tablet
  • RxCUI: 261267 - pioglitazone 30 MG Oral Tablet [Actos]
  • Labeler Name:
    Rebel Distributors Corp.
    Sample Package:
    Start Marketing Date:
    Listing Expiration Date:
    Exclude Flag:
    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.

    Frequently Asked Questions

    What is NDC 21695-148-15?

    The NDC Packaged Code 21695-148-15 is assigned to a package of 15 tablet in 1 bottle of Actos, labeled by Rebel Distributors Corp.. The product's dosage form is and is administered via form.This product is billed for "EA" each discreet unit and contains an estimated amount of 15 billable units per package.

    Is NDC 21695-148 included in the NDC Directory?

    No, Actos with product code 21695-148 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Rebel Distributors Corp. on July 15, 1999 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 21695-148-15?

    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 15.

    What is the 11-digit format for NDC 21695-148-15?

    The 11-digit format is 21695014815. 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