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  5. NDC Package Code: 10122-510-03 Curosurf

NDC Package 10122-510-03 Curosurf

Poractant Alfa Suspension Endotracheal - 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:
10122-510-03
Package Description:
3 mL in 1 VIAL, GLASS
Product Code:
10122-510
Proprietary Name:
Curosurf
Non-Proprietary Name:
Poractant Alfa
Substance Name:
Poractant Alfa
Usage Information:
CUROSURF® (poractant alfa) Intratracheal Suspension is indicated for the rescue treatment of Respiratory Distress Syndrome (RDS) in premature infants.  CUROSURF reduces mortality and pneumothoraces associated with RDS.
11-Digit NDC Billing Format:
10122051003
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
3 ML
NDC to RxNorm Crosswalk:
  • RxCUI: 259216 - poractant alfa 80 MG/ML Intratracheal Suspension
  • RxCUI: 261329 - CUROSURF 80 MG/ML Intratracheal Suspension
  • RxCUI: 261329 - poractant alfa 80 MG/ML Intratracheal Suspension [Curosurf]
  • RxCUI: 261329 - Curosurf 80 MG/ML Intratracheal Suspension
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Chiesi Usa, Inc.
    Dosage Form:
    Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
    Administration Route(s):
  • Endotracheal - Administration directly into the trachea.
    • Active Ingredient(s):
  • PORACTANT ALFA 80 mg/mL
    • Pharmacologic Class(es):
  • Alveolar Surface Tension Reduction - [PE] (Physiologic Effect)
  • Surfactant Activity - [MoA] (Mechanism of Action)
  • Surfactant - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    BLA020744
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    11-18-1999
    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
    10122-510-011.5 mL in 1 VIAL, GLASS

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 10122-510-03?

    The NDC Packaged Code 10122-510-03 is assigned to a package of 3 ml in 1 vial, glass of Curosurf, a human prescription drug labeled by Chiesi Usa, Inc.. The product's dosage form is suspension and is administered via endotracheal form.This product is billed per "ML" milliliter and contains an estimated amount of 3 billable units per package.

    Is NDC 10122-510 included in the NDC Directory?

    Yes, Curosurf with product code 10122-510 is active and included in the NDC Directory. The product was first marketed by Chiesi Usa, Inc. on November 18, 1999 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 10122-510-03?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 3.

    What is the 11-digit format for NDC 10122-510-03?

    The 11-digit format is 10122051003. 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
    5-3-210122-510-035-4-210122-0510-03