NDC 50562-002 Nitrogen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 50562-002-01
Package Description: 6216 L in 1 CYLINDER
NDC Code 50562-002-02
Package Description: 8132 L in 1 CYLINDER
NDC Code 50562-002-03
Package Description: 1456 L in 1 CYLINDER
NDC Code 50562-002-04
Package Description: 3055 L in 1 CYLINDER
NDC Code 50562-002-05
Package Description: 99434 L in 1 CYLINDER
NDC Code 50562-002-06
Package Description: 110606 L in 1 CYLINDER
NDC Code 50562-002-07
Package Description: 147248 L in 1 CYLINDER
NDC Code 50562-002-08
Package Description: 142378 L in 1 CYLINDER
NDC Code 50562-002-09
Package Description: 134053 L in 1 CYLINDER
NDC Code 50562-002-10
Package Description: 180057 L in 1 CYLINDER
NDC Code 50562-002-11
Package Description: 163262 L in 1 CYLINDER
NDC Code 50562-002-12
Package Description: 153498 L in 1 CYLINDER
Product Details
What is NDC 50562-002?
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".