NDC Package 60505-7016-2 Fentanyl

Patch, Extended Release Transdermal - 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:
60505-7016-2
Package Description:
5 POUCH in 1 CARTON / 1 PATCH in 1 POUCH (60505-7016-0) / 72 h in 1 PATCH
Product Code:
Proprietary Name:
Fentanyl
Non-Proprietary Name:
Fentanyl
Substance Name:
Fentanyl
Usage Information:
This medication is used to help relieve severe ongoing pain (such as due to cancer). Fentanyl belongs to a class of drugs known as opioid analgesics. It works in the brain to change how your body feels and responds to pain. Do not use the patch form of fentanyl to relieve pain that is mild or that will go away in a few days. This medication is not for occasional ("as needed") use.
11-Digit NDC Billing Format:
60505701602
NDC to RxNorm Crosswalk:
  • RxCUI: 1603495 - fentaNYL 37.5 MCG/HR 72HR Transdermal System
  • RxCUI: 1603495 - 72 HR fentanyl 0.0375 MG/HR Transdermal System
  • RxCUI: 1603495 - fentanyl 37.5 MCG/HR 3 Day Transdermal Patch
  • RxCUI: 1603498 - fentaNYL 62.5 MCG/HR 72 HR Transdermal System
  • RxCUI: 1603498 - 72 HR fentanyl 0.0625 MG/HR Transdermal System
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Apotex Corp.
    Dosage Form:
    Patch, Extended Release - A drug delivery system in the form of a patch that releases the drug in such a manner that a reduction in dosing frequency compared to that drug presented as a conventional dosage form (e.g., a solution or a prompt drug-releasing, conventional solid dosage form).
    Administration Route(s):
  • Transdermal - Administration through the dermal layer of the skin to the systemic circulation by diffusion.
  • Active Ingredient(s):
    DEA Schedule:
    Schedule II (CII) Substances
    Sample Package:
    No
    FDA Application Number:
    ANDA077449
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-24-2019
    End Marketing Date:
    06-30-2025
    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 60505-7016-2?

    The NDC Packaged Code 60505-7016-2 is assigned to a package of 5 pouch in 1 carton / 1 patch in 1 pouch (60505-7016-0) / 72 h in 1 patch of Fentanyl, a human prescription drug labeled by Apotex Corp.. The product's dosage form is patch, extended release and is administered via transdermal form.

    Is NDC 60505-7016 included in the NDC Directory?

    Yes, Fentanyl with product code 60505-7016 is active and included in the NDC Directory. The product was first marketed by Apotex Corp. on July 24, 2019.

    What is the 11-digit format for NDC 60505-7016-2?

    The 11-digit format is 60505701602. 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
    5-4-160505-7016-25-4-260505-7016-02