NDC Package 70436-026-80 Eptifibatide

Injection 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:
70436-026-80
Package Description:
10 mL in 1 VIAL
Product Code:
Proprietary Name:
Eptifibatide
Non-Proprietary Name:
Eptifibatide
Substance 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 days Severe hypertension (systolic blood pressure >200 mm Hg or diastolic blood pressure >110 mm Hg) not adequately controlled on antihypertensive therapy Major surgery within the preceding 6 weeks History of stroke within 30 days or any history of hemorrhagic stroke Current or planned administration of another parenteral GP IIb/IIIa inhibitor Dependency on renal dialysis Hypersensitivity to eptifibatide injection or any component of the product (hypersensitivity reactions that occurred included anaphylaxis and urticaria).
11-Digit NDC Billing Format:
70436002680
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
10 ML
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
  • RxCUI: 200349 - eptifibatide 75 MG in 100 ML Injection
  • RxCUI: 200349 - 100 ML eptifibatide 0.75 MG/ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Slate Run Pharmaceuticals, Llc
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA209864
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-22-2019
    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.

    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 70436-026-80 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    70436002680J1327Eptifibatide injection5 MG10144

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70436-026-80?

    The NDC Packaged Code 70436-026-80 is assigned to a package of 10 ml in 1 vial of Eptifibatide, a human prescription drug labeled by Slate Run Pharmaceuticals, Llc. The product's dosage form is injection and is administered via intravenous form.This product is billed per "ML" milliliter and contains an estimated amount of 10 billable units per package.

    Is NDC 70436-026 included in the NDC Directory?

    Yes, Eptifibatide with product code 70436-026 is active and included in the NDC Directory. The product was first marketed by Slate Run Pharmaceuticals, Llc on July 22, 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 NDC billing unit for package 70436-026-80?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 10.

    What is the 11-digit format for NDC 70436-026-80?

    The 11-digit format is 70436002680. 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
    5-3-270436-026-805-4-270436-0026-80