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  5. NDC Package Code: 62147-0600-1 Eptifibatide

NDC Package 62147-0600-1 Eptifibatide

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
62147-0600-1
Package Description:
10 mL in 1 VIAL
Product Code:
62147-0600
Proprietary Name:
Eptifibatide
Usage Information:
Treatment with eptifibatide injection is contraindicated in patients with: A history of bleeding diathesis, or evidence of active abnormal bleeding within the previous 30 daysSevere hypertension (systolic blood pressure >200 mm Hg or diastolic blood pressure >110 mm Hg) not adequately controlled on antihypertensive therapyMajor surgery within the preceding 6 weeksHistory of stroke within 30 days or any history of hemorrhagic strokeCurrent or planned administration of another parenteral GP IIb/IIIa inhibitorDependency on renal dialysisHypersensitivity to eptifibatide injection or any component of the product (hypersensitivity reactions that occurred included anaphylaxis and urticaria).
11-Digit NDC Billing Format:
62147060001
NDC to RxNorm Crosswalk:
  • RxCUI: 1736470 - eptifibatide 20 MG in 10 ML Injection
  • RxCUI: 1736470 - 10 ML eptifibatide 2 MG/ML Injection
  • RxCUI: 1736470 - eptifibatide 20 MG per 10 ML Injection
    • Labeler Name:
    Usv Private Limited
    Sample Package:
    No
    Start Marketing Date:
    01-01-2020
    Listing Expiration Date:
    12-31-2021
    Exclude Flag:
    I
    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 62147-0600-1?

    The NDC Packaged Code 62147-0600-1 is assigned to a package of 10 ml in 1 vial of Eptifibatide, labeled by Usv Private Limited. The product's dosage form is and is administered via form.

    Is NDC 62147-0600 included in the NDC Directory?

    No, Eptifibatide with product code 62147-0600 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Usv Private Limited on January 01, 2020 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 62147-0600-1?

    The 11-digit format is 62147060001. 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
    5-4-162147-0600-15-4-262147-0600-01