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  5. NDC Package Code: 70539-001-02 Tymlos

NDC Package 70539-001-02 Tymlos

Abaloparatide Injection, Solution Subcutaneous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
70539-001-02
Package Description:
1 CARTRIDGE in 1 BOX, UNIT-DOSE / 1.56 mL in 1 CARTRIDGE (70539-001-01)
Product Code:
70539-001
Proprietary Name:
Tymlos
Non-Proprietary Name:
Abaloparatide
Substance Name:
Abaloparatide
Usage Information:
Abaloparatide is used to treat bone loss (osteoporosis) for women after menopause who are at high risk of having broken bones (fractures). It is similar to a natural hormone in your body (parathyroid hormone). It works by increasing bone density and strength. This effect helps to decrease the risk of having a fracture. This medication should not be used for children or young adults whose bones are still growing.
11-Digit NDC Billing Format:
70539000102
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1921075 - abaloparatide 3120 MCG in 1.56 ML Pen Injector
  • RxCUI: 1921075 - 1.56 ML abaloparatide 2 MG/ML Pen Injector
  • RxCUI: 1921075 - abaloparatide 2000 MCG/ML per 1.56 ML Pen Injector
  • RxCUI: 1921075 - abaloparatide 3120 MCG per 1.56 ML Pen Injector
  • RxCUI: 1921075 - abaloparatide 80 MCG per 0.04 ML Pen Injector
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Radius Health, Inc.
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    Administration Route(s):
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
    • Active Ingredient(s):
  • ABALOPARATIDE 3.12 mg/1.56mL
    • Pharmacologic Class(es):
  • Parathyroid Hormone-Related Peptide Analog - [EPC] (Established Pharmacologic Class)
  • Parathyroid Hormone-Related Protein - [CS]
    • Sample Package:
    No
    FDA Application Number:
    NDA208743
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    05-01-2017
    Listing Expiration Date:
    12-31-2025
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    70539-001-981 CARTRIDGE in 1 BOX, UNIT-DOSE / 1.56 mL in 1 CARTRIDGE (70539-001-99)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70539-001-02?

    The NDC Packaged Code 70539-001-02 is assigned to a package of 1 cartridge in 1 box, unit-dose / 1.56 ml in 1 cartridge (70539-001-01) of Tymlos, a human prescription drug labeled by Radius Health, Inc.. The product's dosage form is injection, solution and is administered via subcutaneous form.

    Is NDC 70539-001 included in the NDC Directory?

    Yes, Tymlos with product code 70539-001 is active and included in the NDC Directory. The product was first marketed by Radius Health, Inc. on May 01, 2017 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 70539-001-02?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 70539-001-02?

    The 11-digit format is 70539000102. 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
    5-3-270539-001-025-4-270539-0001-02