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  5. NDC Package Code: 70511-141-84 Angiomax Rtu

NDC Package 70511-141-84 Angiomax Rtu

Bivalirudin Injection, 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:
70511-141-84
Package Description:
1 VIAL in 1 PACKAGE / 10 INJECTION, SOLUTION in 1 VIAL
Product Code:
70511-141
Proprietary Name:
Angiomax Rtu
Non-Proprietary Name:
Bivalirudin
Substance Name:
Bivalirudin
Usage Information:
ANGIOMAX RTU is indicated for use as an anticoagulant in patients undergoing percutaneous coronary intervention (PCI), including patients with heparin-induced thrombocytopenia and heparin-induced thrombocytopenia and thrombosis syndrome.
11-Digit NDC Billing Format:
70511014184
NDC to RxNorm Crosswalk:
  • RxCUI: 1997015 - bivalirudin 250 MG in 50 ML Injection
  • RxCUI: 1997015 - 50 ML bivalirudin 5 MG/ML Injection
  • RxCUI: 1997015 - bivalirudin 250 MG (as bivalirudin trifluoroacetate 275 MG) per 50 ML Injection
  • RxCUI: 1997015 - bivalirudin 250 MG per 50 ML Injection
  • RxCUI: 2380558 - ANGIOMAX RTU 250 MG in 50 ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Maia Pharmaceuticals, Inc.
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • BIVALIRUDIN 250 mg/1
    • Pharmacologic Class(es):
  • Anti-coagulant - [EPC] (Established Pharmacologic Class)
  • Direct Thrombin Inhibitor - [EPC] (Established Pharmacologic Class)
  • Thrombin Inhibitors - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    NDA211215
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    08-08-2019
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    70511-141-501 INJECTION, SOLUTION in 1 CARTON

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70511-141-84?

    The NDC Packaged Code 70511-141-84 is assigned to a package of 1 vial in 1 package / 10 injection, solution in 1 vial of Angiomax Rtu, a human prescription drug labeled by Maia Pharmaceuticals, Inc.. The product's dosage form is injection, solution and is administered via intravenous form.

    Is NDC 70511-141 included in the NDC Directory?

    Yes, Angiomax Rtu with product code 70511-141 is active and included in the NDC Directory. The product was first marketed by Maia Pharmaceuticals, Inc. on August 08, 2019 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 70511-141-84?

    The 11-digit format is 70511014184. 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
    5-3-270511-141-845-4-270511-0141-84