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  5. NDC Package Code: 50090-6049-0 Gonal-f Rff

NDC Package 50090-6049-0 Gonal-f Rff

Follitropin Alfa Kit Subcutaneous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
50090-6049-0
Package Description:
1 KIT in 1 KIT * 1 mL in 1 VIAL, SINGLE-USE * 1 mL in 1 SYRINGE, GLASS (44087-9998-1)
Product Code:
50090-6049
Proprietary Name:
Gonal-f Rff
Non-Proprietary Name:
Follitropin Alfa
Usage Information:
Gonal-F RFF is indicated for:
11-Digit NDC Billing Format:
50090604900
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 284419 - GONAL-f RFF 75 UNT Injection
  • RxCUI: 284419 - follitropin alfa 75 UNT Injection [Gonal F]
  • RxCUI: 284419 - Gonal F 75 UNT Injection
  • RxCUI: 562724 - follitropin alfa 75 UNT Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    A-s Medication Solutions
    Dosage Form:
    Kit - A packaged collection of related material.
    Administration Route(s):
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
    • Sample Package:
    No
    FDA Application Number:
    BLA021765
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    03-25-2004
    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.

    Frequently Asked Questions

    What is NDC 50090-6049-0?

    The NDC Packaged Code 50090-6049-0 is assigned to a package of 1 kit in 1 kit * 1 ml in 1 vial, single-use * 1 ml in 1 syringe, glass (44087-9998-1) of Gonal-f Rff, a human prescription drug labeled by A-s Medication Solutions. The product's dosage form is kit and is administered via subcutaneous form.

    Is NDC 50090-6049 included in the NDC Directory?

    Yes, Gonal-f Rff with product code 50090-6049 is active and included in the NDC Directory. The product was first marketed by A-s Medication Solutions on March 25, 2004 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 50090-6049-0?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units.

    What is the 11-digit format for NDC 50090-6049-0?

    The 11-digit format is 50090604900. 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
    5-4-150090-6049-05-4-250090-6049-00