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  5. NDC Package Code: 0004-0191-09 Boniva

NDC Package 0004-0191-09 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:
0004-0191-09
Package Description:
1 SYRINGE, GLASS in 1 CARTON / 3 mL in 1 SYRINGE, GLASS
Product Code:
0004-0191
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:
00004019109
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Labeler Name:
Genentech, Inc.
Sample Package:
No
FDA Application Number:
NDA021858
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
01-06-2006
End Marketing Date:
06-30-2021
Listing Expiration Date:
06-30-2021
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 0004-0191-09?

The NDC Packaged Code 0004-0191-09 is assigned to a package of 1 syringe, glass in 1 carton / 3 ml in 1 syringe, glass of Boniva, labeled by Genentech, Inc.. The product's dosage form is and is administered via form.

Is NDC 0004-0191 included in the NDC Directory?

No, Boniva with product code 0004-0191 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Genentech, Inc. on January 06, 2006 and its listing in the NDC Directory is set to expire on June 30, 2021 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 0004-0191-09?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

What is the 11-digit format for NDC 0004-0191-09?

The 11-digit format is 00004019109. 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
4-4-20004-0191-095-4-200004-0191-09