NDC 0264-4850 Propofol Lipuro

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
0264-4850
Proprietary Name:
Propofol Lipuro
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
B. Braun Medical Inc.
Labeler Code:
0264
Start Marketing Date: [9]
03-12-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 0264-4850-01

Package Description: 10 VIAL in 1 CARTON / 100 mL in 1 VIAL

Product Details

What is NDC 0264-4850?

The NDC code 0264-4850 is assigned by the FDA to the product Propofol Lipuro which is product labeled by B. Braun Medical Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0264-4850-01 10 vial in 1 carton / 100 ml in 1 vial. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

Which are Propofol Lipuro UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Propofol Lipuro Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Propofol Lipuro?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 2559909 - propofol lipid emulsion 1000 MG in 100 ML Injection (EUA)
  • RxCUI: 2559909 - 100 ML propofol lipid emulsion 10 MG/ML Injection
  • RxCUI: 2559909 - propofol lipid emulsion 1000 MG per 100 ML Injection (EUA)
  • RxCUI: 2559909 - propofol-Lipuro 1000 MG per 100 ML Injection (EUA)

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".