NDC Package 0143-9318-10 Norepinephrine Bitartrate

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:
0143-9318-10
Package Description:
10 VIAL in 1 CARTON / 4 mL in 1 VIAL (0143-9318-01)
Product Code:
Proprietary Name:
Norepinephrine Bitartrate
Non-Proprietary Name:
Norepinephrine Bitartrate
Substance Name:
Norepinephrine Bitartrate
Usage Information:
For blood pressure control in certain acute hypotensive states (e.g., pheochromocytomectomy, sympathectomy, poliomyelitis, spinal anesthesia, myocardial infarction, septicemia, blood transfusion, and drug reactions).As an adjunct in the treatment of cardiac arrest and profound hypotension.
11-Digit NDC Billing Format:
00143931810
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 242969 - norepinephrine bitartrate 4 MG in 4 mL Injection
  • RxCUI: 242969 - 4 ML norepinephrine 1 MG/ML Injection
  • RxCUI: 242969 - norepinephrine (as bitartrate) 4 MG per 4 ML Injection
  • RxCUI: 242969 - norepinephrine 4 MG per 4 ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hikma Pharmaceuticals Usa Inc.
    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):
    Sample Package:
    No
    FDA Application Number:
    ANDA203662
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-01-2018
    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 0143-9318-10?

    The NDC Packaged Code 0143-9318-10 is assigned to a package of 10 vial in 1 carton / 4 ml in 1 vial (0143-9318-01) of Norepinephrine Bitartrate, a human prescription drug labeled by Hikma Pharmaceuticals Usa Inc.. The product's dosage form is injection and is administered via intravenous form.

    Is NDC 0143-9318 included in the NDC Directory?

    Yes, Norepinephrine Bitartrate with product code 0143-9318 is active and included in the NDC Directory. The product was first marketed by Hikma Pharmaceuticals Usa Inc. on August 01, 2018 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 0143-9318-10?

    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 0143-9318-10?

    The 11-digit format is 00143931810. 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 4-4-2 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
    4-4-20143-9318-105-4-200143-9318-10