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  5. NDC Package Code: 25021-826-67 Zoledronic Acid

NDC Package 25021-826-67 Zoledronic Acid

Injection, Solution Intravenous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    3. Other Packages
    4. Frequently Asked Questions

Package Information

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:
25021-826-67
Package Description:
1 BAG in 1 CARTON / 100 mL in 1 BAG
Product Code:
25021-826
Proprietary Name:
Zoledronic Acid
Non-Proprietary Name:
Zoledronic Acid
Substance 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:
25021082667
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1114085 - zoledronic acid 4 MG in 100 ML Injection
  • RxCUI: 1114085 - 100 ML zoledronic acid 0.04 MG/ML Injection
  • RxCUI: 1114085 - zoledronic acid 4 MG per 100 ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Sagent Pharmaceuticals
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • ZOLEDRONIC ACID .04 mg/mL
  • ZOLEDRONIC ACID .04 mg/mL
    • Pharmacologic Class(es):
  • Bisphosphonate - [EPC] (Established Pharmacologic Class)
  • Diphosphonates - [CS]
  • Bisphosphonate - [EPC] (Established Pharmacologic Class)
  • Diphosphonates - [CS]
    • Sample Package:
    No
    FDA Application Number:
    NDA203231
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    03-02-2013
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    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.

    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 25021-826-67 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    25021082667J3489Zoledronic acid 1mg1 MG100144

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    25021-826-821 BAG in 1 CARTON / 100 mL in 1 BAG

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 25021-826-67?

    The NDC Packaged Code 25021-826-67 is assigned to a package of 1 bag in 1 carton / 100 ml in 1 bag of Zoledronic Acid, a human prescription drug labeled by Sagent Pharmaceuticals. The product's dosage form is injection, solution and is administered via intravenous form.

    Is NDC 25021-826 included in the NDC Directory?

    Yes, Zoledronic Acid with product code 25021-826 is active and included in the NDC Directory. The product was first marketed by Sagent Pharmaceuticals on March 02, 2013 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 25021-826-67?

    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 25021-826-67?

    The 11-digit format is 25021082667. 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
    5-3-225021-826-675-4-225021-0826-67