NDC Package 43066-555-24 Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride

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

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:
43066-555-24
Package Description:
24 BAG in 1 CARTON / 50 mL in 1 BAG
Product Code:
Proprietary Name:
Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride
Non-Proprietary Name:
Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride
Substance Name:
Dexmedetomidine Hydrochloride
Usage Information:
None
11-Digit NDC Billing Format:
43066055524
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1718906 - dexmedeTOMIDine HCl 200 MCG in 50 ML Injection
  • RxCUI: 1718906 - 50 ML dexmedetomidine 0.004 MG/ML Injection
  • RxCUI: 1718906 - dexmedetomidine (as dexmedetomidine HCl) 200 MCG per 50 ML Injection
  • RxCUI: 1718909 - dexmedeTOMIDine HCl 400 MCG in 100 ML Injection
  • RxCUI: 1718909 - 100 ML dexmedetomidine 0.004 MG/ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Baxter Healthcare Corporation
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
  • Sample Package:
    No
    FDA Application Number:
    ANDA208532
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-27-2019
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N

    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 43066-555-24?

    The NDC Packaged Code 43066-555-24 is assigned to a package of 24 bag in 1 carton / 50 ml in 1 bag of Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride, a human prescription drug labeled by Baxter Healthcare Corporation. The product's dosage form is injection and is administered via intravenous form.

    Is NDC 43066-555 included in the NDC Directory?

    Yes, Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride with product code 43066-555 is active and included in the NDC Directory. The product was first marketed by Baxter Healthcare Corporation on August 27, 2019 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 43066-555-24?

    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 43066-555-24?

    The 11-digit format is 43066055524. 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
    5-3-243066-555-245-4-243066-0555-24