NDC 10006-001 Oxygen

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:
10006-001
Proprietary Name:
Oxygen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
10006
Start Marketing Date: [9]
01-01-1936
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 10006-001?

The NDC code 10006-001 is assigned by the FDA to the product Oxygen which is product labeled by Acetylene Oxygen Company. The product's dosage form is . The product is distributed in 19 packages with assigned NDC codes 10006-001-01 103 l in 1 cylinder , 10006-001-02 150 l in 1 cylinder , 10006-001-03 255 l in 1 cylinder , 10006-001-04 426 l in 1 cylinder , 10006-001-05 671 l in 1 cylinder , 10006-001-06 610 l in 1 cylinder , 10006-001-07 1140 l in 1 cylinder , 10006-001-08 1500 l in 1 cylinder , 10006-001-09 3462 l in 1 cylinder , 10006-001-10 6900 l in 1 cylinder , 10006-001-11 9310 l in 1 cylinder , 10006-001-12 21 l in 1 dewar , 10006-001-13 31 l in 1 dewar , 10006-001-14 41 l in 1 dewar , 10006-001-15 46 l in 1 dewar , 10006-001-16 160 l in 1 dewar , 10006-001-17 180 l in 1 dewar , 10006-001-18 176 l in 1 dewar , 10006-001-19 225 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 UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Oxygen?

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".