NDC Package 81293-000-04 Mycophenolate Mofetil

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:
81293-000-04
Package Description:
4 VIAL in 1 CARTON / 20 mL in 1 VIAL
Product Code:
Proprietary Name:
Mycophenolate Mofetil
Non-Proprietary Name:
Mycophenolate Mofetil
Substance Name:
Mycophenolate Mofetil
Usage Information:
Mycophenolate is used in combination with other medications to keep your body from attacking and rejecting your transplanted organ (such as kidney, liver, heart). It belongs to a class of medications called immunosuppressants. It works by weakening your body's defense system (immune system) to help your body accept the new organ as if it were your own.
11-Digit NDC Billing Format:
81293000004
NDC to RxNorm Crosswalk:
  • RxCUI: 311881 - mycophenolate mofetil 500 MG Injection
  • RxCUI: 311881 - mycophenolate mofetil (as mycophenolate mofetil hydrochloride) 500 MG Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Steriscience Pte. 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:
    ANDA216390
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-30-2023
    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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 81293-000-04?

    The NDC Packaged Code 81293-000-04 is assigned to a package of 4 vial in 1 carton / 20 ml in 1 vial of Mycophenolate Mofetil, a human prescription drug labeled by Steriscience Pte. Limited. The product's dosage form is injection, powder, lyophilized, for solution and is administered via intravenous form.

    Is NDC 81293-000 included in the NDC Directory?

    Yes, Mycophenolate Mofetil with product code 81293-000 is active and included in the NDC Directory. The product was first marketed by Steriscience Pte. Limited on April 30, 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 81293-000-04?

    The 11-digit format is 81293000004. 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 5-3-2 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
    5-3-281293-000-045-4-281293-0000-04