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  5. NDC Package Code: 72266-147-10 Etomidate

NDC Package 72266-147-10 Etomidate

Etomidate Injection Solution 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:
72266-147-10
Package Description:
10 VIAL in 1 CARTON / 20 mL in 1 VIAL (72266-147-01)
Product Code:
72266-147
Proprietary Name:
Etomidate
Non-Proprietary Name:
Etomidate Injection
Substance Name:
Etomidate
Usage Information:
Etomidate Injection, USP is indicated by intravenous injection for the induction of general anesthesia. When considering use of etomidate, the usefulness of its hemodynamic properties (see CLINICAL PHARMACOLOGY) should be weighed against the high frequency of transient skeletal muscle movements (see ADVERSE REACTIONS). Intravenous etomidate is also indicated for the supplementation of subpotent anesthetic agents, such as nitrous oxide in oxygen, during maintenance of anesthesia for short operative procedures such as dilation and curettage or cervical conization.
11-Digit NDC Billing Format:
72266014710
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1654006 - etomidate 20 MG in 10 ML Injection
  • RxCUI: 1654006 - 10 ML etomidate 2 MG/ML Injection
  • RxCUI: 1654006 - etomidate 20 MG per 10 ML Injection
  • RxCUI: 1654008 - etomidate 40 MG in 20 ML Injection
  • RxCUI: 1654008 - 20 ML etomidate 2 MG/ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Fosun Pharma Usa Inc
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • ETOMIDATE 2 mg/mL
    • Pharmacologic Class(es):
  • General Anesthesia - [PE] (Physiologic Effect)
  • General Anesthetic - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA209058
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    09-03-2019
    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 72266-147-10?

    The NDC Packaged Code 72266-147-10 is assigned to a package of 10 vial in 1 carton / 20 ml in 1 vial (72266-147-01) of Etomidate, a human prescription drug labeled by Fosun Pharma Usa Inc. The product's dosage form is solution and is administered via intravenous form.

    Is NDC 72266-147 included in the NDC Directory?

    Yes, Etomidate with product code 72266-147 is active and included in the NDC Directory. The product was first marketed by Fosun Pharma Usa Inc on September 03, 2019 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 72266-147-10?

    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 72266-147-10?

    The 11-digit format is 72266014710. 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
    5-3-272266-147-105-4-272266-0147-10