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  5. NDC Package Code: 84549-535-50 Intralipid

NDC Package 84549-535-50 Intralipid

I.v. Fat Emulsion Emulsion Intravenous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
84549-535-50
Package Description:
500 mL in 1 BAG
Product Code:
84549-535
Proprietary Name:
Intralipid
Non-Proprietary Name:
I.v. Fat Emulsion
Substance Name:
Soybean Oil
Usage Information:
This product is used to provide calories to patients who are getting their nutrition through an injection into the vein. Calories are needed to provide the body with energy so that the body can work properly. This product is also used to provide a certain nutrient (essential fatty acids) to people who do not have enough of it. This product helps to prevent or reverse the signs of this deficiency (e.g., scaly skin, poor growth, poor wound healing).
11-Digit NDC Billing Format:
84549053550
Product Type:
Human Prescription Drug
Labeler Name:
Propharma Distribution
Dosage Form:
Emulsion - A dosage form consisting of a two-phase system comprised of at least two immiscible liquids1, one of which is dispersed as droplets (internal or dispersed phase) within the other liquid (external or continuous phase), generally stabilized with one or more emulsifying agents. (Note: Emulsion is used as a dosage form term unless a more specific term is applicable, e.g. cream, lotion, ointment.)
Administration Route(s):
Intravenous - Administration within or into a vein or veins.
Active Ingredient(s):
SOYBEAN OIL 20 g/100mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
NDA018449
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
04-01-2004
Listing Expiration Date:
12-31-2026
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 84549-535-50?

The NDC Packaged Code 84549-535-50 is assigned to a package of 500 ml in 1 bag of Intralipid, a human prescription drug labeled by Propharma Distribution. The product's dosage form is emulsion and is administered via intravenous form.

Is NDC 84549-535 included in the NDC Directory?

Yes, Intralipid with product code 84549-535 is active and included in the NDC Directory. The product was first marketed by Propharma Distribution on April 01, 2004 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 84549-535-50?

The 11-digit format is 84549053550. 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
5-3-284549-535-505-4-284549-0535-50