NDC Package 50090-4569-1 Propofol

View Billable Units, 11-Digit Format, RxNorm

Package Information
Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:

50090-4569-1

Package Description:

50 mL in 1 VIAL

Product Code:

50090-4569

Proprietary 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 Emulsion Indication Approved Patient Population Initiation and maintenance of Monitored Anesthesia Care (MAC) sedation Adults only Combined sedation and regional anesthesia Adults only (see PRECAUTIONS) Induction of General Anesthesia Patients greater than or equal to 3 years of age Maintenance of General Anesthesia Patients greater than or equal to 2 months of age Intensive 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 Injectable Emulsion is not recommended for use in nursing mothers because propofol 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:

50090456901

Billing Unit:

ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.

NDC to RxNorm Crosswalk:

50 ML

NDC to RxNorm Crosswalk:

RxCUI: 1808222 - propofol 500 MG in 50 ML Injection

RxCUI: 1808222 - 50 ML propofol 10 MG/ML Injection

RxCUI: 1808222 - propofol 500 MG per 50 ML Injection

Labeler Name:

A-s Medication Solutions

Sample Package:

Start Marketing Date:

01-07-2016

Listing Expiration Date:

12-31-2022

Exclude Flag:

Code Structure:

50090 - A-s Medication Solutions
- 50090-4569 - Propofol
  - 50090-4569-1 - 50 mL in 1 VIAL

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 50090-4569-1?

The NDC Packaged Code 50090-4569-1 is assigned to a package of 50 ml in 1 vial of Propofol, labeled by A-s Medication Solutions. The product's dosage form is and is administered via form.This product is billed per "ML" milliliter and contains an estimated amount of 50 billable units per package.

Is NDC 50090-4569 included in the NDC Directory?

No, Propofol with product code 50090-4569 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by A-s Medication Solutions on January 07, 2016 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 50090-4569-1?

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 50.

What is the 11-digit format for NDC 50090-4569-1?

The 11-digit format is 50090456901. 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 5-4-1 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-4-1	50090-4569-1	5-4-2	50090-4569-01

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