NDC 51758-004 Oxygen 4c21e554-d402-480d-896d-8185c05c7863

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:
51758-004
Proprietary Name:
Oxygen 4c21e554-d402-480d-896d-8185c05c7863
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Gases Plus Norco, Llc
Labeler Code:
51758
Start Marketing Date: [9]
09-01-2008
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 51758-004-01

Package Description: 165 L in 1 DEWAR

NDC Code 51758-004-02

Package Description: 185 L in 1 DEWAR

NDC Code 51758-004-03

Package Description: 196 L in 1 DEWAR

Product Details

What is NDC 51758-004?

The NDC code 51758-004 is assigned by the FDA to the product Oxygen 4c21e554-d402-480d-896d-8185c05c7863 which is product labeled by Gases Plus Norco, Llc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 51758-004-01 165 l in 1 dewar , 51758-004-02 185 l in 1 dewar , 51758-004-03 196 l in 1 dewar . 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 4c21e554-d402-480d-896d-8185c05c7863 UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Oxygen 4c21e554-d402-480d-896d-8185c05c7863?

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 code indicates a single concept unique identifier (RXCUI) is associated with this product:

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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".