NDC Package 81298-9659-3 Norepinephrine

Norepinephrine Bitartrate 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:
81298-9659-3
Package Description:
10 POUCH in 1 BOX / 1 BAG in 1 POUCH (81298-9659-1) / 250 mL in 1 BAG
Product Code:
Proprietary Name:
Norepinephrine
Non-Proprietary Name:
Norepinephrine Bitartrate
Substance Name:
Norepinephrine Bitartrate
Usage Information:
Norepinephrine in Sodium Chloride Injection is indicated to raise blood pressure in adult patients with severe, acute hypotension.
11-Digit NDC Billing Format:
81298965903
NDC to RxNorm Crosswalk:
  • RxCUI: 2475337 - norepinephrine bitartrate 4 MG in 250 ML Injection
  • RxCUI: 2475337 - 250 ML norepinephrine 0.016 MG/ML Injection
  • RxCUI: 2475337 - norepinephrine (as bitartrate) 4 MG per 250 ML Injection
  • RxCUI: 2475340 - norepinephrine bitartrate 8 MG in 250 ML Injection
  • RxCUI: 2475340 - 250 ML norepinephrine 0.032 MG/ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Long Grove Pharmaceuticals, Llc
    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.
  • Sample Package:
    No
    FDA Application Number:
    NDA214628
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    02-02-2024
    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.

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    Frequently Asked Questions

    What is NDC 81298-9659-3?

    The NDC Packaged Code 81298-9659-3 is assigned to a package of 10 pouch in 1 box / 1 bag in 1 pouch (81298-9659-1) / 250 ml in 1 bag of Norepinephrine, a human prescription drug labeled by Long Grove Pharmaceuticals, Llc. The product's dosage form is solution and is administered via intravenous form.

    Is NDC 81298-9659 included in the NDC Directory?

    Yes, Norepinephrine with product code 81298-9659 is active and included in the NDC Directory. The product was first marketed by Long Grove Pharmaceuticals, Llc on February 02, 2024 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 11-digit format for NDC 81298-9659-3?

    The 11-digit format is 81298965903. 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 5-4-1 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
    5-4-181298-9659-35-4-281298-9659-03