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  5. NDC Package Code: 67877-241-31 Alendronate Sodium

NDC Package 67877-241-31 Alendronate Sodium

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
67877-241-31
Package Description:
1 BLISTER PACK in 1 CARTON / 4 TABLET in 1 BLISTER PACK
Product Code:
67877-241
Proprietary Name:
Alendronate Sodium
Usage Information:
Alendronate is used to prevent and treat certain types of bone loss (osteoporosis) in adults. Osteoporosis causes bones to become thinner and break more easily. Your chance of developing osteoporosis increases as you age, after menopause, or if you are taking corticosteroid medications (such as prednisone) for a long time. This medication works by slowing bone loss. This effect helps maintain strong bones and reduce the risk of broken bones (fractures). Alendronate belongs to a class of drugs called bisphosphonates.
11-Digit NDC Billing Format:
67877024131
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
Labeler Name:
Ascend Laboratories, Llc
Sample Package:
No
FDA Application Number:
ANDA090258
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
09-01-2011
End Marketing Date:
10-28-2015
Listing Expiration Date:
10-28-2015
Exclude Flag:
D
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
67877-241-332 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 67877-241-31?

The NDC Packaged Code 67877-241-31 is assigned to a package of 1 blister pack in 1 carton / 4 tablet in 1 blister pack of Alendronate Sodium, labeled by Ascend Laboratories, Llc. The product's dosage form is and is administered via form.

Is NDC 67877-241 included in the NDC Directory?

No, Alendronate Sodium with product code 67877-241 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Ascend Laboratories, Llc on September 01, 2011 and its listing in the NDC Directory is set to expire on October 28, 2015 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 67877-241-31?

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 1.

What is the 11-digit format for NDC 67877-241-31?

The 11-digit format is 67877024131. 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
5-3-267877-241-315-4-267877-0241-31