NDC 58420-002 Nitrogen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 58420-002-01
Package Description: 4 L in 1 CYLINDER
NDC Code 58420-002-02
Package Description: 5 L in 1 CYLINDER
NDC Code 58420-002-03
Package Description: 25 L in 1 CYLINDER
NDC Code 58420-002-04
Package Description: 30 L in 1 CYLINDER
NDC Code 58420-002-05
Package Description: 80 L in 1 CYLINDER
NDC Code 58420-002-06
Package Description: 145 L in 1 CYLINDER
NDC Code 58420-002-07
Package Description: 166 L in 1 CYLINDER
NDC Code 58420-002-08
Package Description: 233 L in 1 CYLINDER
NDC Code 58420-002-09
Package Description: 245 L in 1 CYLINDER
NDC Code 58420-002-10
Package Description: 267 L in 1 CYLINDER
NDC Code 58420-002-11
Package Description: 396 L in 1 CYLINDER
NDC Code 58420-002-12
Package Description: 538 L in 1 CYLINDER
NDC Code 58420-002-13
Package Description: 651 L in 1 CYLINDER
NDC Code 58420-002-14
Package Description: 1189 L in 1 CYLINDER
NDC Code 58420-002-15
Package Description: 1614 L in 1 CYLINDER
NDC Code 58420-002-16
Package Description: 2463 L in 1 CYLINDER
NDC Code 58420-002-17
Package Description: 3313 L in 1 CYLINDER
NDC Code 58420-002-18
Package Description: 4021 L in 1 CYLINDER
NDC Code 58420-002-19
Package Description: 6513 L in 1 CYLINDER
NDC Code 58420-002-20
Package Description: 7107 L in 1 CYLINDER
NDC Code 58420-002-21
Package Description: 8608 L in 1 CYLINDER
Product Details
What is NDC 58420-002?
Which are Nitrogen UNII Codes?
The UNII codes for the active ingredients in this product are:
- NITROGEN (UNII: N762921K75)
- NITROGEN (UNII: N762921K75) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Nitrogen?
- RxCUI: 348624 - nitrogen 99.2 % Gas for Inhalation
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[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".