NDC Package 67184-0570-2 Amikacin Sulfate

Injection, 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:
67184-0570-2
Package Description:
10 VIAL, GLASS in 1 CARTON / 4 mL in 1 VIAL, GLASS (67184-0570-1)
Product Code:
Proprietary Name:
Amikacin Sulfate
Non-Proprietary Name:
Amikacin Sulfate
Substance Name:
Amikacin Sulfate
Usage Information:
This medication is used to prevent or treat a wide variety of bacterial infections. Amikacin belongs to a class of drugs known as aminoglycoside antibiotics. It works by stopping the growth of bacteria.
11-Digit NDC Billing Format:
67184057002
NDC to RxNorm Crosswalk:
  • RxCUI: 1723156 - amikacin sulfate 500 MG in 2 ML Injection
  • RxCUI: 1723156 - 2 ML amikacin 250 MG/ML Injection
  • RxCUI: 1723156 - amikacin (as amikacin sulfate) 500 MG per 2 ML Injection
  • RxCUI: 1723160 - amikacin sulfate 1 GM in 4 ML Injection
  • RxCUI: 1723160 - 4 ML amikacin 250 MG/ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Qilu Pharmaceutical Co., Ltd.
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    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:
    ANDA218146
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    03-19-2024
    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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 67184-0570-2?

    The NDC Packaged Code 67184-0570-2 is assigned to a package of 10 vial, glass in 1 carton / 4 ml in 1 vial, glass (67184-0570-1) of Amikacin Sulfate, a human prescription drug labeled by Qilu Pharmaceutical Co., Ltd.. The product's dosage form is injection, solution and is administered via intramuscular; intravenous form.

    Is NDC 67184-0570 included in the NDC Directory?

    Yes, Amikacin Sulfate with product code 67184-0570 is active and included in the NDC Directory. The product was first marketed by Qilu Pharmaceutical Co., Ltd. on March 19, 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 67184-0570-2?

    The 11-digit format is 67184057002. 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
    5-4-167184-0570-25-4-267184-0570-02