NDC 49972-004 Nitrous Oxide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 49972-004-01
Package Description: 17987 L in 1 CYLINDER
NDC Code 49972-004-02
Package Description: 15770 L in 1 CYLINDER
NDC Code 49972-004-03
Package Description: 14784 L in 1 CYLINDER
NDC Code 49972-004-04
Package Description: 9610 L in 1 CYLINDER
NDC Code 49972-004-05
Package Description: 7885 L in 1 CYLINDER
NDC Code 49972-004-06
Package Description: 4928 L in 1 CYLINDER
NDC Code 49972-004-07
Package Description: 2664 L in 1 CYLINDER
NDC Code 49972-004-08
Package Description: 1725 L in 1 CYLINDER
NDC Code 49972-004-09
Package Description: 1232 L in 1 CYLINDER
NDC Code 49972-004-10
Package Description: 986 L in 1 CYLINDER
NDC Code 49972-004-11
Package Description: 493 L in 1 CYLINDER
NDC Code 49972-004-12
Package Description: 246 L in 1 CYLINDER
NDC Code 49972-004-13
Package Description: 17248 L in 1 DEWAR
NDC Code 49972-004-14
Package Description: 1971 L in 1 DEWAR
NDC Code 49972-004-15
Package Description: 46816 L in 1 DEWAR
NDC Code 49972-004-16
Package Description: 88458 L in 1 DEWAR
NDC Code 49972-004-17
Package Description: 93632 L in 1 DEWAR
NDC Code 49972-004-18
Package Description: 107667 L in 1 DEWAR
NDC Code 49972-004-19
Package Description: 130099 L in 1 DEWAR
NDC Code 49972-004-20
Package Description: 141680 L in 1 DEWAR
Product Details
What is NDC 49972-004?
Which are Nitrous Oxide UNII Codes?
The UNII codes for the active ingredients in this product are:
- NITROUS OXIDE (UNII: K50XQU1029)
- NITROUS OXIDE (UNII: K50XQU1029) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Nitrous Oxide?
- RxCUI: 312022 - nitrous oxide 99 % 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".