NDC 57472-003 Nitrous Oxide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 57472-003-01
Package Description: 2464 L in 1 CYLINDER
NDC Code 57472-003-02
Package Description: 4928 L in 1 CYLINDER
NDC Code 57472-003-03
Package Description: 7392 L in 1 CYLINDER
NDC Code 57472-003-04
Package Description: 91168 L in 1 CYLINDER
NDC Code 57472-003-05
Package Description: 16016 L in 1 CYLINDER
NDC Code 57472-003-06
Package Description: 15770 L in 1 CYLINDER
NDC Code 57472-003-07
Package Description: 3696 L in 1 CYLINDER
NDC Code 57472-003-08
Package Description: 12320 L in 1 CYLINDER
NDC Code 57472-003-09
Package Description: 17989 L in 1 CYLINDER
NDC Code 57472-003-10
Package Description: 1724 L in 1 CYLINDER
NDC Code 57472-003-11
Package Description: 985 L in 1 CYLINDER
NDC Code 57472-003-12
Package Description: 370 L in 1 CYLINDER
Product Details
What is NDC 57472-003?
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: 347166 - nitrous oxide 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".