NDC Package 57881-333-32 Abstral

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
57881-333-32
Package Description:
8 BLISTER PACK in 1 CARTON / 4 TABLET in 1 BLISTER PACK (57881-333-04)
Product Code:
Proprietary Name:
Abstral
Usage Information:
This medication is used to help relieve sudden (breakthrough) pain in people who are already taking opioid medication around-the-clock for cancer pain. 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. This medication should not be used to relieve mild or short-term pain (such as due to headache/migraine, dental procedures, surgery).
11-Digit NDC Billing Format:
57881033332
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
8 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1053647 - fentaNYL 100 MCG Sublingual Tablet
  • RxCUI: 1053647 - fentanyl 0.1 MG Sublingual Tablet
  • RxCUI: 1053647 - fentanyl (as fentanyl citrate) 100 MCG Sublingual Tablet
  • RxCUI: 1053651 - ABSTRAL 100 MCG Sublingual Tablet
  • RxCUI: 1053651 - fentanyl 0.1 MG Sublingual Tablet [Abstral]
  • Labeler Name:
    Galena Biopharma, Inc.
    Sample Package:
    No
    Start Marketing Date:
    08-08-2013
    Listing Expiration Date:
    12-31-2019
    Exclude Flag:
    I
    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 57881-333-32?

    The NDC Packaged Code 57881-333-32 is assigned to a package of 8 blister pack in 1 carton / 4 tablet in 1 blister pack (57881-333-04) of Abstral, labeled by Galena Biopharma, Inc.. The product's dosage form is and is administered via form.This product is billed for "EA" each discreet unit and contains an estimated amount of 8 billable units per package.

    Is NDC 57881-333 included in the NDC Directory?

    No, Abstral with product code 57881-333 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Galena Biopharma, Inc. on August 08, 2013 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 57881-333-32?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 8.

    What is the 11-digit format for NDC 57881-333-32?

    The 11-digit format is 57881033332. 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
    5-3-257881-333-325-4-257881-0333-32