NDC Package 70771-1683-6 Micafungin

Injection, Powder, Lyophilized, 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:
70771-1683-6
Package Description:
10 VIAL in 1 CARTON / 5 mL in 1 VIAL (70771-1683-1)
Product Code:
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:
70771168306
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:
    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):
    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:
    12-31-2024
    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.

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    Frequently Asked Questions

    What is NDC 70771-1683-6?

    The NDC Packaged Code 70771-1683-6 is assigned to a package of 10 vial in 1 carton / 5 ml in 1 vial (70771-1683-1) 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 70771-1683 included in the NDC Directory?

    Yes, Micafungin with product code 70771-1683 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, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 70771-1683-6?

    The 11-digit format is 70771168306. 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
    5-4-170771-1683-65-4-270771-1683-06