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  5. NDC Package Code: 44567-811-10 Esmolol Hydrochloride In Water

NDC Package 44567-811-10 Esmolol Hydrochloride In Water

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

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    3. 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:
44567-811-10
Package Description:
10 BAG in 1 CARTON / 250 mL in 1 BAG
Product Code:
44567-811
Proprietary Name:
Esmolol Hydrochloride In Water
Non-Proprietary Name:
Esmolol Hydrochloride
Substance Name:
Esmolol Hydrochloride
Usage Information:
Each bag is for single patient use only and does not contain any preservatives. Once drug has been withdrawn from ready-to-use bag, the infusion of the bag contents should commence immediately and complete within 24 hours. Any unused portion is to be discarded.Do not remove unit from overwrap until ready to use. Do not use if overwrap has been previously opened or damaged. The overwrap is a moisture barrier. The inner bag maintains sterility of the solution. Tear overwrap at notch and remove premixed bag.Check for minute leaks by squeezing the inner bag firmly. If leaks are found, discard solution, as sterility may be impaired. Do not use unless the solution is clear (colorless to light yellow) and the seal is intact.Preparation for intravenous administration:•Use aseptic technique.•Suspend premixed bag from eyelet support.•Remove plastic protector from delivery port at bottom of bag.•Attach administration set.•Refer to complete directions accompanying set.Do not use plastic containers in series connections. Such use could result in an embolism due to residual air being drawn from the primary container before administration of the fluid from the secondary container is completed.Esmolol Hydrochloride is not compatible with Sodium Bicarbonate (5%) solution (limited stability) or furosemide (precipitation). Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Premixed Bag •The medication port is to be used solely for withdrawing an initial bolus from the bag. •Use aseptic technique when withdrawing the bolus dose. •Do not add any additional medications to the bag.Figure 1. Dual Port Bag Compatibility with Commonly Used Intravenous Fluids Esmolol hydrochloride was tested for compatibility with ten commonly used intravenous fluids at a final concentration of 10 mg esmolol hydrochloride per mL. Esmolol hydrochloride was found to be compatible with the following solutions and was stable for at least 24 hours at controlled room temperature or under refrigeration: •Dextrose (5%) Injection, USP •Dextrose (5%) in Lactated Ringer’s Injection •Dextrose (5%) in Ringer’s Injection •Dextrose (5%) and Sodium Chloride (0.45%) Injection, USP •Dextrose (5%) and Sodium Chloride (0.9%) Injection, USP •Lactated Ringer’s Injection, USP •Potassium Chloride (40 mEq/liter) in Dextrose (5%) Injection, USP •Sodium Chloride (0.45%) Injection, USP •Sodium Chloride (0.9%) Injection, USP
11-Digit NDC Billing Format:
44567081110
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1736541 - esmolol HCl 2500 MG in 250 ML Injection
  • RxCUI: 1736541 - 250 ML esmolol hydrochloride 10 MG/ML Injection
  • RxCUI: 1736541 - esmolol HCl 2500 MG per 250 ML Injection
  • RxCUI: 979432 - esmolol HCl 2000 MG in 100 ML Injection
  • RxCUI: 979432 - 100 ML esmolol hydrochloride 20 MG/ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Wg Critical Care, Llc
    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.
    • Active Ingredient(s):
  • ESMOLOL HYDROCHLORIDE 10 mg/mL
    • Pharmacologic Class(es):
  • Adrenergic beta-Antagonists - [MoA] (Mechanism of Action)
  • beta-Adrenergic Blocker - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    NDA205703
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    12-04-2017
    Listing Expiration Date:
    12-31-2025
    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 44567-811-10 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    44567081110J1806Inj esmolol hcl wg crit care10 MG250102502500

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 44567-811-10?

    The NDC Packaged Code 44567-811-10 is assigned to a package of 10 bag in 1 carton / 250 ml in 1 bag of Esmolol Hydrochloride In Water, a human prescription drug labeled by Wg Critical Care, Llc. The product's dosage form is injection and is administered via intravenous form.

    Is NDC 44567-811 included in the NDC Directory?

    Yes, Esmolol Hydrochloride In Water with product code 44567-811 is active and included in the NDC Directory. The product was first marketed by Wg Critical Care, Llc on December 04, 2017 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 44567-811-10?

    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 44567-811-10?

    The 11-digit format is 44567081110. 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
    5-3-244567-811-105-4-244567-0811-10