NDC 58420-005 Air

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:
58420-005
Proprietary Name:
Air
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Airgas Intermountain Inc
Labeler Code:
58420
Start Marketing Date: [9]
01-01-1958
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 58420-005-01

Package Description: 3311 L in 1 CYLINDER

NDC Code 58420-005-02

Package Description: 4075 L in 1 CYLINDER

NDC Code 58420-005-03

Package Description: 6622 L in 1 CYLINDER

NDC Code 58420-005-04

Package Description: 7386 L in 1 CYLINDER

NDC Code 58420-005-05

Package Description: 8801 L in 1 CYLINDER

NDC Code 58420-005-06

Package Description: 1528 L in 1 CYLINDER

NDC Code 58420-005-07

Package Description: 2321 L in 1 CYLINDER

NDC Code 58420-005-08

Package Description: 425 L in 1 CYLINDER

NDC Code 58420-005-09

Package Description: 623 L in 1 CYLINDER

NDC Code 58420-005-10

Package Description: 651 L in 1 CYLINDER

Product Details

What is NDC 58420-005?

The NDC code 58420-005 is assigned by the FDA to the product Air which is product labeled by Airgas Intermountain Inc. The product's dosage form is . The product is distributed in 10 packages with assigned NDC codes 58420-005-01 3311 l in 1 cylinder , 58420-005-02 4075 l in 1 cylinder , 58420-005-03 6622 l in 1 cylinder , 58420-005-04 7386 l in 1 cylinder , 58420-005-05 8801 l in 1 cylinder , 58420-005-06 1528 l in 1 cylinder , 58420-005-07 2321 l in 1 cylinder , 58420-005-08 425 l in 1 cylinder , 58420-005-09 623 l in 1 cylinder , 58420-005-10 651 l in 1 cylinder . 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 Air 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".