NDC 61755-005-02 Eylea

Aflibercept

  1. Labeler Index
  2. Regeneron Pharmaceuticals, Inc.
  3. 61755-005
  4. NDC Code: 61755-005-02 Eylea

NDC Package Code 61755-005-02

The NDC 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.

Field Name Field Value
NDC Code 61755-005-02
Package Description 1 VIAL, SINGLE-USE in 1 CARTON > .05 mL in 1 VIAL, SINGLE-USE
Proprietary Name Eylea What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name Aflibercept What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Drug Uses 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 NDC Format for Billing
For insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.
Billing Unit ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Product Type Human Prescription Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
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)
  • AFLIBERCEPT 40 mg/mL
Pharmacological Class(es)
  • Vascular Endothelial Growth Factor Inhibitor - [EPC] (Established Pharmacologic Class)
  • Vascular Endothelial Growth Factor Inhibitors - [MoA] (Mechanism of Action)
Sample Package No Sample Package?
This field Indicates whether this package is a sample packaging or not.
Marketing Category BLA - A product marketed under an approved Biologic License Application. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
FDA Application Number BLA125387 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Start Marketing Date 11-21-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

NDC Code Structure

  • 61755 - Regeneron Pharmaceuticals, Inc.
    • 61755-005 - Eylea
      • 61755-005-02 - 1 VIAL, SINGLE-USE in 1 CARTON

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.

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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

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Other Product Packages

The following packages are also available for Eylea with product NDC 61755-005.

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.