NDC Package 47335-615-44 Norepinephrine Bitartrate

Injection, Solution, Concentrate 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:
47335-615-44
Package Description:
10 VIAL, SINGLE-DOSE in 1 CARTON / 4 mL in 1 VIAL, SINGLE-DOSE
Product Code:
Proprietary Name:
Norepinephrine Bitartrate
Non-Proprietary Name:
Norepinephrine Bitartrate
Substance Name:
Norepinephrine Bitartrate
Usage Information:
Norepinephrine bitartrate injection is indicated to raise blood pressure in adult patients with severe, acute hypotension.
11-Digit NDC Billing Format:
47335061544
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:
    Sun Pharmaceutical Industries, Inc.
    Dosage Form:
    Injection, Solution, Concentrate - A sterile preparation for parenteral use which, upon the addition of suitable solvents, yields a solution conforming in all respects to the requirements for Injections.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA211980
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-01-2021
    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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 47335-615-44?

    The NDC Packaged Code 47335-615-44 is assigned to a package of 10 vial, single-dose in 1 carton / 4 ml in 1 vial, single-dose of Norepinephrine Bitartrate, a human prescription drug labeled by Sun Pharmaceutical Industries, Inc.. The product's dosage form is injection, solution, concentrate and is administered via intravenous form.

    Is NDC 47335-615 included in the NDC Directory?

    Yes, Norepinephrine Bitartrate with product code 47335-615 is active and included in the NDC Directory. The product was first marketed by Sun Pharmaceutical Industries, Inc. on July 01, 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 NDC billing unit for package 47335-615-44?

    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 47335-615-44?

    The 11-digit format is 47335061544. 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
    5-3-247335-615-445-4-247335-0615-44