NDC Package 60505-6120-6 Micafungin

Injection, Powder, Lyophilized, For Solution Intravenous - View Billable Units, 11-Digit Format, RxNorm

Package Information
NDC HCPCS Crosswalk
Frequently Asked Questions

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:

60505-6120-6

Package Description:

10 VIAL, SINGLE-USE in 1 CARTON / 5 mL in 1 VIAL, SINGLE-USE

Product Code:

60505-6120

Proprietary Name:

Micafungin

Non-Proprietary Name:

Micafungin

Substance Name:

Micafungin

Usage Information:

Micafungin for injection is indicated for: Treatment of Candidemia, Acute Disseminated Candidiasis, Candida Peritonitis and Abscesses in adult and pediatric patients 4 months of age and older [see Clinical Studies (14.1) and Use in Specific Populations (8.4)]Treatment of Candidemia, Acute Disseminated Candidiasis, Candida Peritonitis and Abscesses without meningoencephalitis and/or ocular dissemination in pediatric patients younger than 4 months of age [see Use in Specific Populations (8.4)]. Treatment of Esophageal Candidiasis in adult and pediatric patients 4 months of age and older [see Clinical Studies (14.2)]. Prophylaxis of Candida Infections in adult and pediatric patients 4 months of age and older undergoing hematopoietic stem cell transplantation [see Clinical Studies (14.3)]. Limitations of UseThe safety and effectiveness of micafungin for injection has not been established for the treatment of candidemia with meningoencephalitis and/or ocular dissemination in pediatric patients younger than 4 months of age as a higher dose may be needed [see Use in Specific Populations (8.4)].Micafungin for injection has not been adequately studied in patients with endocarditis, osteomyelitis and meningoencephalitis due to Candida. The efficacy of micafungin for injection against infections caused by fungi other than Candida has not been established.

11-Digit NDC Billing Format:

60505612006

Billing Unit:

EA - Billing unit of "each" is used when the product is dispensed in discreet units.

NDC to RxNorm Crosswalk:

1 EA

NDC to RxNorm Crosswalk:

RxCUI: 861379 - micafungin sodium 50 MG Injection

RxCUI: 861379 - micafungin 50 MG Injection

RxCUI: 861379 - micafungin 50 MG (equivalent to micafungin sodium 50.86 MG) Injection

RxCUI: 861383 - micafungin sodium 100 MG Injection

RxCUI: 861383 - micafungin 100 MG Injection

Product Type:

Human Prescription Drug

Labeler Name:

Apotex Corp.

Dosage Form:

Injection, Powder, Lyophilized, For Solution - A dosage form intended for the solution prepared by lyophilization ("freeze drying"), a process which involves the removal of water from products in the frozen state at extremely low pressures; this is intended for subsequent addition of liquid to create a solution that conforms in all respects to the requirements for Injections.

Administration Route(s):

Intravenous - Administration within or into a vein or veins.

Active Ingredient(s):

MICAFUNGIN 20 mg/mL

Pharmacologic Class(es):

Echinocandin Antifungal - [EPC] (Established Pharmacologic Class)

Lipopeptides - [CS]

Sample Package:

FDA Application Number:

ANDA208366

Marketing Category:

ANDA - A product marketed under an approved Abbreviated New Drug Application.

Start Marketing Date:

02-12-2021

End Marketing Date:

07-31-2024

Exclude Flag:

Code Structure:

60505 - Apotex Corp.
- 60505-6120 - Micafungin
  - 60505-6120-6 - 10 VIAL, SINGLE-USE in 1 CARTON / 5 mL in 1 VIAL, SINGLE-USE

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.

NDC HCPCS Crosswalk

This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

NDC 60505-6120-6 HCPCS crosswalk information with package details and bill units information.

NDC Billing Code	HCPCS Code	HCPCS Code Desc.	Dosage	Package Size	Package Quantity	Billable Units	Billable Units / Pkg
60505612006	J2248	Micafungin sodium injection	1 MG	1	10	100	1000

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 60505-6120-6?

The NDC Packaged Code 60505-6120-6 is assigned to a package of 10 vial, single-use in 1 carton / 5 ml in 1 vial, single-use of Micafungin, a human prescription drug labeled by Apotex Corp.. The product's dosage form is injection, powder, lyophilized, for solution and is administered via intravenous form.This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package.

Is NDC 60505-6120 included in the NDC Directory?

Yes, Micafungin with product code 60505-6120 is active and included in the NDC Directory. The product was first marketed by Apotex Corp. on February 12, 2021.

What is the NDC billing unit for package 60505-6120-6?

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 1.

What is the 11-digit format for NDC 60505-6120-6?

The 11-digit format is 60505612006. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-4-1	60505-6120-6	5-4-2	60505-6120-06

Table of Contents