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  5. NDC Package Code: 0004-0186-83 Boniva

NDC Package 0004-0186-83 Boniva

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
0004-0186-83
Package Description:
1 BLISTER PACK in 1 BOX / 3 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
0004-0186
Proprietary Name:
Boniva
Usage Information:
Ibandronate is used to prevent and treat certain types of bone loss (osteoporosis). Osteoporosis causes bones to become thinner and break more easily. Your chance of developing osteoporosis increases after menopause, as you age, or if you take corticosteroid medications (such as prednisone) for long periods. This medication works by slowing bone loss to help maintain strong bones and reduce the risk of broken bones (fractures). Ibandronate belongs to a class of medications called bisphosphonates.
11-Digit NDC Billing Format:
00004018683
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:
Genentech, Inc.
Sample Package:
No
FDA Application Number:
NDA021455
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
03-24-2005
End Marketing Date:
07-31-2023
Listing Expiration Date:
07-31-2023
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.

Frequently Asked Questions

What is NDC 0004-0186-83?

The NDC Packaged Code 0004-0186-83 is assigned to a package of 1 blister pack in 1 box / 3 tablet, film coated in 1 blister pack of Boniva, labeled by Genentech, Inc.. The product's dosage form is and is administered via form.

Is NDC 0004-0186 included in the NDC Directory?

No, Boniva with product code 0004-0186 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Genentech, Inc. on March 24, 2005 and its listing in the NDC Directory is set to expire on July 31, 2023 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 0004-0186-83?

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 0004-0186-83?

The 11-digit format is 00004018683. 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
4-4-20004-0186-835-4-200004-0186-83