NDC Package 60505-6144-4 Cefepime

Injection, Powder, For Solution Intramuscular; 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:
60505-6144-4
Package Description:
10 VIAL, SINGLE-DOSE in 1 CARTON / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
Product Code:
Proprietary Name:
Cefepime
Non-Proprietary Name:
Cefepime
Substance Name:
Cefepime Hydrochloride
Usage Information:
Cefepime is used to treat a wide variety of bacterial infections. This medication belongs to a class of drugs known as cephalosporin antibiotics. It works by stopping the growth of bacteria.
11-Digit NDC Billing Format:
60505614404
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
10 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1665088 - cefepime 2 GM Injection
  • RxCUI: 1665088 - cefepime 2000 MG Injection
  • RxCUI: 1665088 - cefepime 2 GM (as cefepime HCl) Injection
  • RxCUI: 1665093 - cefepime 1 GM Injection
  • RxCUI: 1665093 - cefepime 1000 MG Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Apotex Corp.
    Dosage Form:
    Injection, Powder, For Solution - A sterile preparation intended for reconstitution to form a solution for parenteral use.
    Administration Route(s):
  • Intramuscular - Administration within a muscle.
  • Intravenous - Administration within or into a vein or veins.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA203704
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-14-2017
    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 60505-6144-4?

    The NDC Packaged Code 60505-6144-4 is assigned to a package of 10 vial, single-dose in 1 carton / 1 injection, powder, for solution in 1 vial, single-dose of Cefepime, a human prescription drug labeled by Apotex Corp.. The product's dosage form is injection, powder, for solution and is administered via intramuscular; intravenous form.

    Is NDC 60505-6144 included in the NDC Directory?

    Yes, Cefepime with product code 60505-6144 is active and included in the NDC Directory. The product was first marketed by Apotex Corp. on November 14, 2017 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 60505-6144-4?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 10.

    What is the 11-digit format for NDC 60505-6144-4?

    The 11-digit format is 60505614404. 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
    5-4-160505-6144-45-4-260505-6144-04