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  5. NDC Package Code: 47335-035-40 Zoledronic Acid

NDC Package 47335-035-40 Zoledronic Acid

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 .

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:
47335-035-40
Package Description:
1 VIAL in 1 CARTON / 5 mL in 1 VIAL
Product Code:
47335-035
Proprietary Name:
Zoledronic Acid
Usage Information:
This medication is used to treat high blood calcium levels (hypercalcemia) that may occur with cancer. Zoledronic acid is also used with cancer chemotherapy to treat bone problems that may occur with multiple myeloma and other types of cancer (such as breast, lung) that have spread to the bones. Zoledronic acid belongs to a class of drugs known as bisphosphonates. It lowers high blood calcium levels by reducing the amount of calcium released from your bones into your blood. It also works by slowing the breakdown of your bones by cancer to prevent bone fractures.
11-Digit NDC Billing Format:
47335003540
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Labeler Name:
Sun Pharma Global Fze
Sample Package:
No
FDA Application Number:
ANDA202746
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
03-04-2013
End Marketing Date:
09-30-2015
Listing Expiration Date:
09-30-2015
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.

Frequently Asked Questions

What is NDC 47335-035-40?

The NDC Packaged Code 47335-035-40 is assigned to a package of 1 vial in 1 carton / 5 ml in 1 vial of Zoledronic Acid, labeled by Sun Pharma Global Fze. The product's dosage form is and is administered via form.

Is NDC 47335-035 included in the NDC Directory?

The product was first marketed by Sun Pharma Global Fze on March 04, 2013 and its listing in the NDC Directory is set to expire on September 30, 2015 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 47335-035-40?

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 47335-035-40?

The 11-digit format is 47335003540. 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
5-3-247335-035-405-4-247335-0035-40