NDC Package 0002-8147-01 Humatrope

Somatropin Kit Intramuscular; Subcutaneous - 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:
0002-8147-01
Package Description:
1 TRAY in 1 CARTON / 1 KIT in 1 TRAY * 2.88 mL in 1 CARTRIDGE (0002-7554-01) * 2.88 mL in 1 SYRINGE (0002-7618-01)
Product Code:
Proprietary Name:
Humatrope
Non-Proprietary Name:
Somatropin
Usage Information:
Various brands of this medication are used for the treatment of one of the following medical conditions: growth failure, growth hormone deficiency, intestinal disorder (short bowel syndrome) or HIV-related weight loss or wasting. Somatropin is also used to increase height in children with certain disorders (such as Noonan syndrome, Turner syndrome, idiopathic short stature).
11-Digit NDC Billing Format:
00002814701
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 582969 - somatropin 12 MG Cartridge
  • RxCUI: 582971 - Humatrope 12 MG Cartridge
  • RxCUI: 582971 - somatropin 12 MG Cartridge [Humatrope]
  • RxCUI: 582974 - somatropin 24 MG Cartridge
  • RxCUI: 582976 - Humatrope 24 MG Cartridge
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Eli Lilly And Company
    Dosage Form:
    Kit - A packaged collection of related material.
    Administration Route(s):
  • Intramuscular - Administration within a muscle.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
  • Sample Package:
    No
    FDA Application Number:
    BLA019640
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    01-27-2006
    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 0002-8147-01?

    The NDC Packaged Code 0002-8147-01 is assigned to a package of 1 tray in 1 carton / 1 kit in 1 tray * 2.88 ml in 1 cartridge (0002-7554-01) * 2.88 ml in 1 syringe (0002-7618-01) of Humatrope, a human prescription drug labeled by Eli Lilly And Company. The product's dosage form is kit and is administered via intramuscular; subcutaneous form.

    Is NDC 0002-8147 included in the NDC Directory?

    Yes, Humatrope with product code 0002-8147 is active and included in the NDC Directory. The product was first marketed by Eli Lilly And Company on January 27, 2006 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 0002-8147-01?

    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 0002-8147-01?

    The 11-digit format is 00002814701. 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
    4-4-20002-8147-015-4-200002-8147-01