NDC Package 61755-005-02 Eylea

Aflibercept Injection, Solution Intravitreal - 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:
61755-005-02
Package Description:
1 VIAL, SINGLE-USE in 1 CARTON / .05 mL in 1 VIAL, SINGLE-USE
Product Code:
Proprietary Name:
Eylea
Non-Proprietary Name:
Aflibercept
Substance Name:
Aflibercept
Usage Information:
Aflibercept is used to treat certain serious eye conditions (such as wet age-related macular degeneration, diabetic retinopathy/macular edema, macular edema following retinal vein occlusion). This medication can help preserve vision and prevent blindness. Aflibercept belongs to a class of drugs known as growth factor inhibitors. It works by slowing the growth of abnormal new blood vessels in the eye and decreasing leakage from these blood vessels.
11-Digit NDC Billing Format:
61755000502
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1232154 - aflibercept 2 MG in 0.05 ML Injection
  • RxCUI: 1232154 - 0.05 ML aflibercept 40 MG/ML Injection
  • RxCUI: 1232154 - aflibercept 2 MG per 0.05 ML Intravitreal Injection
  • RxCUI: 1232159 - EYLEA 2 MG in 0.05 ML Injection
  • RxCUI: 1232159 - 0.05 ML aflibercept 40 MG/ML Injection [Eylea]
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Regeneron 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):
  • Intravitreal - Administration within the vitreous body of the eye.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    BLA125387
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    11-21-2011
    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 61755-005-02 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    61755000502J0178Aflibercept injection1 MG0.05122

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    61755-005-011 SYRINGE, GLASS in 1 CARTON / .05 mL in 1 SYRINGE, GLASS
    61755-005-541 SYRINGE, GLASS in 1 CARTON / .05 mL in 1 SYRINGE, GLASS
    61755-005-551 VIAL, SINGLE-USE in 1 CARTON / .05 mL in 1 VIAL, SINGLE-USE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 61755-005-02?

    The NDC Packaged Code 61755-005-02 is assigned to a package of 1 vial, single-use in 1 carton / .05 ml in 1 vial, single-use of Eylea, a human prescription drug labeled by Regeneron Pharmaceuticals, Inc.. The product's dosage form is injection, solution and is administered via intravitreal form.

    Is NDC 61755-005 included in the NDC Directory?

    Yes, Eylea with product code 61755-005 is active and included in the NDC Directory. The product was first marketed by Regeneron Pharmaceuticals, Inc. on November 21, 2011 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 61755-005-02?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 61755-005-02?

    The 11-digit format is 61755000502. 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
    5-3-261755-005-025-4-261755-0005-02