NDC Package 0074-0039-56 Orilissa

Elagolix Tablet, Film Coated Oral - 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:
0074-0039-56
Package Description:
4 BLISTER PACK in 1 CARTON / 14 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Orilissa
Non-Proprietary Name:
Elagolix
Substance Name:
Elagolix Sodium
Usage Information:
This medication is used by women to help relieve moderate to severe pain due to a condition called endometriosis. Endometriosis is the growth of tissue that normally lines the inside of the womb (uterus) in a different place, such as on the outside surface of the uterus, on the ovaries, or on other organs. This condition may cause symptoms such as painful/heavy/irregular menstrual periods, pain during or after sex, or infertility. Elagolix works by decreasing your body's production of certain hormones (luteinizing hormone, follicle-stimulating hormone), which leads to lower amounts of female sex hormones (estrogens). These lower levels may help decrease some symptoms of endometriosis.
11-Digit NDC Billing Format:
00074003956
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
4 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 2049852 - elagolix 150 MG Oral Tablet
  • RxCUI: 2049852 - elagolix 150 MG (as elagolix sodium 155.2 MG) Oral Tablet
  • RxCUI: 2049858 - Orilissa 150 MG Oral Tablet
  • RxCUI: 2049858 - elagolix 150 MG Oral Tablet [Orilissa]
  • RxCUI: 2049860 - elagolix 200 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Abbvie Inc.
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA210450
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    07-23-2018
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    0074-0039-141 BLISTER PACK in 1 CARTON / 14 TABLET, FILM COATED in 1 BLISTER PACK

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0074-0039-56?

    The NDC Packaged Code 0074-0039-56 is assigned to a package of 4 blister pack in 1 carton / 14 tablet, film coated in 1 blister pack of Orilissa, a human prescription drug labeled by Abbvie Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 0074-0039 included in the NDC Directory?

    Yes, Orilissa with product code 0074-0039 is active and included in the NDC Directory. The product was first marketed by Abbvie Inc. on July 23, 2018 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 0074-0039-56?

    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 4.

    What is the 11-digit format for NDC 0074-0039-56?

    The 11-digit format is 00074003956. 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 4-4-2 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
    4-4-20074-0039-565-4-200074-0039-56