NDC Package 65145-128-10 Etomidate

Injection, Solution 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:
65145-128-10
Package Description:
10 VIAL, SINGLE-DOSE in 1 CARTON / 20 mL in 1 VIAL, SINGLE-DOSE (65145-128-01)
Product Code:
Proprietary Name:
Etomidate
Non-Proprietary Name:
Etomidate
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:
65145012810
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:
    Caplin Steriles Limited
    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.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA215028
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    03-15-2021
    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.

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    Frequently Asked Questions

    What is NDC 65145-128-10?

    The NDC Packaged Code 65145-128-10 is assigned to a package of 10 vial, single-dose in 1 carton / 20 ml in 1 vial, single-dose (65145-128-01) of Etomidate, a human prescription drug labeled by Caplin Steriles Limited. The product's dosage form is injection, solution and is administered via intravenous form.

    Is NDC 65145-128 included in the NDC Directory?

    Yes, Etomidate with product code 65145-128 is active and included in the NDC Directory. The product was first marketed by Caplin Steriles Limited on March 15, 2021 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 11-digit format for NDC 65145-128-10?

    The 11-digit format is 65145012810. 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
    5-3-265145-128-105-4-265145-0128-10