NDC Package 67184-1004-1 Cefepime

Cefepime Hydrochloride Injection, Powder, For 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:
67184-1004-1
Package Description:
10 VIAL in 1 CARTON / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product Code:
Proprietary Name:
Cefepime
Non-Proprietary Name:
Cefepime Hydrochloride
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:
67184100401
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:
    Qilu Pharmaceutical Co., Ltd.
    Dosage Form:
    Injection, Powder, For Solution - A sterile preparation intended for reconstitution to form a solution for parenteral use.
    Administration Route(s):
  • 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:
    02-01-2016
    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 67184-1004-1?

    The NDC Packaged Code 67184-1004-1 is assigned to a package of 10 vial in 1 carton / 1 injection, powder, for solution in 1 vial of Cefepime, a human prescription drug labeled by Qilu Pharmaceutical Co., Ltd.. The product's dosage form is injection, powder, for solution and is administered via intravenous form.

    Is NDC 67184-1004 included in the NDC Directory?

    Yes, Cefepime with product code 67184-1004 is active and included in the NDC Directory. The product was first marketed by Qilu Pharmaceutical Co., Ltd. on February 01, 2016 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 67184-1004-1?

    The 11-digit format is 67184100401. 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
    5-4-167184-1004-15-4-267184-1004-01