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  5. NDC Package Code: 70771-1684-1 Micafungin

NDC Package 70771-1684-1 Micafungin

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

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
70771-1684-1
Package Description:
1 VIAL in 1 CARTON / 5 mL in 1 VIAL
Product Code:
70771-1684
Proprietary Name:
Micafungin
Non-Proprietary Name:
Micafungin
Substance Name:
Micafungin Sodium
Usage Information:
This medication is used to treat a variety of fungal infections. It is also used to prevent fungal infections in patients who are having a stem cell transplant. Micafungin belongs to a class of drugs known as echinocandins. It works by stopping the growth of fungi.
11-Digit NDC Billing Format:
70771168401
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Zydus Lifesciences Limited
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 SODIUM 20 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA215241
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
04-10-2023
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
70771-1684-610 VIAL in 1 CARTON / 5 mL in 1 VIAL

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 70771-1684-1?

The NDC Packaged Code 70771-1684-1 is assigned to a package of 1 vial in 1 carton / 5 ml in 1 vial of Micafungin, a human prescription drug labeled by Zydus Lifesciences Limited. The product's dosage form is injection, powder, lyophilized, for solution and is administered via intravenous form.

Is NDC 70771-1684 included in the NDC Directory?

Yes, Micafungin with product code 70771-1684 is active and included in the NDC Directory. The product was first marketed by Zydus Lifesciences Limited on April 10, 2023 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 70771-1684-1?

The 11-digit format is 70771168401. 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
5-4-170771-1684-15-4-270771-1684-01