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  4. NDC Product Code: 11054-999 Oxygen

NDC 11054-999 Oxygen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 11054-999?
  4. Active Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
11054-999
Proprietary Name:
Oxygen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Airgas Usa, Llc
Labeler Code:
11054
Product Label ID:
243411f1-b376-5193-e054-00144ff88e88
Start Marketing Date: [9]
01-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 11054-999-01

Package Description: 46 L in 1 TANK

NDC Code 11054-999-02

Package Description: 30 L in 1 TANK

NDC Code 11054-999-03

Package Description: 45 L in 1 TANK

NDC Code 11054-999-04

Package Description: 41 L in 1 TANK

NDC Code 11054-999-05

Package Description: 40 L in 1 TANK

Product Details

What is NDC 11054-999?

The NDC code 11054-999 is assigned by the FDA to the product Oxygen which is product labeled by Airgas Usa, Llc. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 11054-999-01 46 l in 1 tank , 11054-999-02 30 l in 1 tank , 11054-999-03 45 l in 1 tank , 11054-999-04 41 l in 1 tank , 11054-999-05 40 l in 1 tank . 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 Oxygen UNII Codes?

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

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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".