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  5. NDC Package Code: 55150-266-05 Zoledronic Acid

NDC Package 55150-266-05 Zoledronic Acid

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

Table of Contents

    1. Package Information
    2. 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:
55150-266-05
Package Description:
1 VIAL, SINGLE-DOSE in 1 CARTON / 5 mL in 1 VIAL, SINGLE-DOSE
Product Code:
55150-266
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:
55150026605
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 351114 - zoledronic acid 4 MG in 5 ML Injection
  • RxCUI: 351114 - 5 ML zoledronic acid 0.8 MG/ML Injection
  • RxCUI: 351114 - zoledronic acid 4 MG per 5 ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Auromedics Pharma Llc
    Dosage Form:
    Injection, Solution, Concentrate - A sterile preparation for parenteral use which, upon the addition of suitable solvents, yields a solution conforming in all respects to the requirements for Injections.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • ZOLEDRONIC ACID 4 mg/5mL
    • Pharmacologic Class(es):
  • Bisphosphonate - [EPC] (Established Pharmacologic Class)
  • Diphosphonates - [CS]
    • Sample Package:
    No
    FDA Application Number:
    ANDA207751
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    09-26-2016
    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.

    Frequently Asked Questions

    What is NDC 55150-266-05?

    The NDC Packaged Code 55150-266-05 is assigned to a package of 1 vial, single-dose in 1 carton / 5 ml in 1 vial, single-dose of Zoledronic Acid, a human prescription drug labeled by Auromedics Pharma Llc. The product's dosage form is injection, solution, concentrate and is administered via intravenous form.

    Is NDC 55150-266 included in the NDC Directory?

    Yes, Zoledronic Acid with product code 55150-266 is active and included in the NDC Directory. The product was first marketed by Auromedics Pharma Llc on September 26, 2016 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 55150-266-05?

    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 55150-266-05?

    The 11-digit format is 55150026605. 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
    5-3-255150-266-055-4-255150-0266-05