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  5. NDC Package Code: 71288-157-10 Thiotepa

NDC Package 71288-157-10 Thiotepa

Injection, Powder, For Solution Intracavitary; Intravenous; Intravesical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
71288-157-10
Package Description:
1 VIAL, SINGLE-DOSE in 1 CARTON / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
Product Code:
71288-157
Proprietary Name:
Thiotepa
Non-Proprietary Name:
Thiotepa
Substance Name:
Thiotepa
Usage Information:
Thiotepa is used to treat cancer. It works by slowing or stopping the growth of cancer cells. Thiotepa is often given into the bladder to treat bladder cancer. Thiotepa is also used with other medications to prevent rejection of a stem cell transplant.
11-Digit NDC Billing Format:
71288015710
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: 1660004 - thiotepa 100 MG Injection
  • RxCUI: 1660004 - TSPA 100 MG Injection
  • RxCUI: 1660009 - thiotepa 15 MG Injection
  • RxCUI: 1660009 - TSPA 15 MG Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Meitheal Pharmaceuticals Inc
    Dosage Form:
    Injection, Powder, For Solution - A sterile preparation intended for reconstitution to form a solution for parenteral use.
    Administration Route(s):
  • Intracavitary - Administration within a non-pathologic cavity, such as that of the cervix, uterus, or penis, or such as that which is formed as the result of a wound.
  • Intravenous - Administration within or into a vein or veins.
  • Intravesical - Administration within the bladder.
    • Active Ingredient(s):
  • THIOTEPA 100 mg/1
    • Pharmacologic Class(es):
  • Alkylating Activity - [MoA] (Mechanism of Action)
  • Alkylating Drug - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA216037
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-26-2023
    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 71288-157-10?

    The NDC Packaged Code 71288-157-10 is assigned to a package of 1 vial, single-dose in 1 carton / 1 injection, powder, for solution in 1 vial, single-dose of Thiotepa, a human prescription drug labeled by Meitheal Pharmaceuticals Inc. The product's dosage form is injection, powder, for solution and is administered via intracavitary; intravenous; intravesical form.This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package.

    Is NDC 71288-157 included in the NDC Directory?

    Yes, Thiotepa with product code 71288-157 is active and included in the NDC Directory. The product was first marketed by Meitheal Pharmaceuticals Inc on December 26, 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 NDC billing unit for package 71288-157-10?

    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 71288-157-10?

    The 11-digit format is 71288015710. 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
    5-3-271288-157-105-4-271288-0157-10