NDC Package 0074-2282-03 Lupron Depot-ped

Leuprolide Acetate Kit - 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:
0074-2282-03
Package Description:
1 KIT in 1 CARTON * 1 mL in 1 SYRINGE * 1 SWAB in 1 PACKET
Product Code:
Proprietary Name:
Lupron Depot-ped
Non-Proprietary Name:
Leuprolide Acetate
Usage Information:
Leuprolide is used to stop early puberty (precocious puberty) in children. It helps to delay sexual development (such as growth of the breasts/testicles) and the start of menstrual periods. It also helps slow down early bone growth to increase the likelihood of reaching normal adult height. Leuprolide works by decreasing the amount of sex hormones that a child's body makes (estrogen in girls, testosterone in boys).
11-Digit NDC Billing Format:
00074228203
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 1115447 - leuprolide acetate 11.25 MG in 1 ML (pediatric 1 month) Prefilled Syringe
  • RxCUI: 1115447 - 1 ML leuprolide acetate 11.25 MG/ML Prefilled Syringe
  • RxCUI: 1115447 - leuprolide acetate 11.25 MG per 1 ML (pediatric 1 month) Prefilled Syringe
  • RxCUI: 1115447 - leuprolide acetate 11.25 MG per 1 ML Prefilled Syringe
  • RxCUI: 1115449 - LUPRON DEPOT-PED 11.25 MG in 1 ML (1 month) Prefilled Syringe
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Abbvie Inc.
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    NDA020263
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    04-16-1993
    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 0074-2282-03?

    The NDC Packaged Code 0074-2282-03 is assigned to a package of 1 kit in 1 carton * 1 ml in 1 syringe * 1 swab in 1 packet of Lupron Depot-ped, a human prescription drug labeled by Abbvie Inc.. The product's dosage form is kit and is administered via form.

    Is NDC 0074-2282 included in the NDC Directory?

    Yes, Lupron Depot-ped with product code 0074-2282 is active and included in the NDC Directory. The product was first marketed by Abbvie Inc. on April 16, 1993 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 0074-2282-03?

    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 0074-2282-03?

    The 11-digit format is 00074228203. 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
    4-4-20074-2282-035-4-200074-2282-03