NDC Package 58160-824-15 Priorix

Measels,Mumps,And Rubella Vaccine,Live 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:
58160-824-15
Package Description:
1 KIT in 1 CARTON * .5 mL in 1 VIAL (58160-831-03) * .5 mL in 1 SYRINGE (58160-833-02)
Product Code:
Proprietary Name:
Priorix
Non-Proprietary Name:
Measels, Mumps, And Rubella Vaccine, Live
Usage Information:
PRIORIX is a vaccine indicated for active immunization for the prevention of measles, mumps, and rubella in individuals 12 months of age and older.
11-Digit NDC Billing Format:
58160082415
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 2603508 - measles, mumps, and rubella virus vaccine live (generic for Priorix) 0.5 ML Injection
  • RxCUI: 2603508 - 0.5 ML measles virus vaccine live, attenuated Schwarz strain 5024 UNT/ML / mumps virus vaccine live, RIT-4385 strain 31684 UNT/ML / rubella virus vaccine live (Wistar RA 27-3 strain) 3990 UNT/ML Injection
  • RxCUI: 2603514 - PRIORIX vaccine 0.5 ML Injection
  • RxCUI: 2603514 - 0.5 ML measles virus vaccine live, attenuated Schwarz strain 5024 UNT/ML / mumps virus vaccine live, RIT-4385 strain 31684 UNT/ML / rubella virus vaccine live (Wistar RA 27-3 strain) 3990 UNT/ML Injection [Priorix]
  • RxCUI: 2603514 - Priorix Measles, Mumps, and Rubella Virus Vaccine Live 0.5 ML Injection
  • Product Type:
    Vaccine
    Labeler Name:
    Glaxosmithkline Biologicals Sa
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    BLA125748
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    06-03-2022
    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.

    Frequently Asked Questions

    What is NDC 58160-824-15?

    The NDC Packaged Code 58160-824-15 is assigned to a package of 1 kit in 1 carton * .5 ml in 1 vial (58160-831-03) * .5 ml in 1 syringe (58160-833-02) of Priorix, a vaccine label labeled by Glaxosmithkline Biologicals Sa. The product's dosage form is kit and is administered via form.

    Is NDC 58160-824 included in the NDC Directory?

    Yes, Priorix with product code 58160-824 is active and included in the NDC Directory. The product was first marketed by Glaxosmithkline Biologicals Sa on June 03, 2022 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 58160-824-15?

    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 58160-824-15?

    The 11-digit format is 58160082415. 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
    5-3-258160-824-155-4-258160-0824-15