NDC Package 0409-4699-24 Propofol

Injection, Emulsion Intravenous - 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:
0409-4699-24
Package Description:
10 VIAL in 1 TRAY / 100 mL in 1 VIAL (0409-4699-54)
Product Code:
Proprietary Name:
Propofol
Non-Proprietary Name:
Propofol
Substance Name:
Propofol
Usage Information:
Propofol injectable emulsion is an IV general anesthetic and sedation drug that can be used as described in the table below. TABLE 3. INDICATIONS FOR PROPOFOL INJECTABLE EMULSIONIndicationApproved Patient PopulationInitiation and maintenance of Monitored Anesthesia Care (MAC) sedation Adults onlyCombined sedation and regional anesthesia Adults only (see PRECAUTIONS)Induction of General Anesthesia Patients greater than or equal to 3 years of ageMaintenance of General Anesthesia Patients greater than or equal to 2 months of ageIntensive Care Unit (ICU) sedation of intubated, mechanically ventilated patients Adults onlySafety, effectiveness and dosing guidelines for propofol injectable emulsion have not been established for MAC Sedation in the pediatric population; therefore, it is not recommended for this use (see PRECAUTIONS, Pediatric Use). Propofol injectable emulsion is not recommended for induction of anesthesia below the age of 3 years or for maintenance of anesthesia below the age of 2 months because its safety and effectiveness have not been established in those populations. In the Intensive Care Unit (ICU), propofol injectable emulsion can be administered to intubated, mechanically ventilated adult patients to provide continuous sedation and control of stress responses only by persons skilled in the medical management of critically ill patients and trained in cardiovascular resuscitation and airway management. Propofol injectable emulsion is not indicated for use in Pediatric ICU sedation since the safety of this regimen has not been established (see PRECAUTIONS, Pediatric Use). Propofol injectable emulsion is not recommended for obstetrics, including Cesarean section deliveries. Propofol injectable emulsion crosses the placenta, and as with other general anesthetic agents, the administration of propofol injectable emulsion may be associated with neonatal depression (see PRECAUTIONS). Propofol is not recommended for use in nursing mothers because propofol injectable emulsion has been reported to be excreted in human milk, and the effects of oral absorption of small amounts of propofol are not known (see PRECAUTIONS).
11-Digit NDC Billing Format:
00409469924
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1808217 - propofol 1000 MG in 100 ML Injection
  • RxCUI: 1808217 - 100 ML propofol 10 MG/ML Injection
  • RxCUI: 1808217 - propofol 1000 MG per 100 ML Injection
  • RxCUI: 1808222 - propofol 500 MG in 50 ML Injection
  • RxCUI: 1808222 - 50 ML propofol 10 MG/ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hospira, Inc.
    Dosage Form:
    Injection, Emulsion - An emulsion consisting of a sterile, pyrogen-free preparation intended to be administered parenterally.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA077908
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-03-2006
    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.

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    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 0409-4699-24 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    00409469924J2704Inj, propofol, 10 mg10 MG100101001000

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    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    0409-4699-305 VIAL in 1 CARTON / 20 mL in 1 VIAL (0409-4699-50)
    0409-4699-3320 VIAL in 1 TRAY / 50 mL in 1 VIAL (0409-4699-53)

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    Frequently Asked Questions

    What is NDC 0409-4699-24?

    The NDC Packaged Code 0409-4699-24 is assigned to a package of 10 vial in 1 tray / 100 ml in 1 vial (0409-4699-54) of Propofol, a human prescription drug labeled by Hospira, Inc.. The product's dosage form is injection, emulsion and is administered via intravenous form.

    Is NDC 0409-4699 included in the NDC Directory?

    Yes, Propofol with product code 0409-4699 is active and included in the NDC Directory. The product was first marketed by Hospira, Inc. on April 03, 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 0409-4699-24?

    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 0409-4699-24?

    The 11-digit format is 00409469924. 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
    4-4-20409-4699-245-4-200409-4699-24