NDC 25543-012 Nitrous Oxide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 25543-012-01
Package Description: 368 L in 1 CYLINDER
NDC Code 25543-012-02
Package Description: 934 L in 1 CYLINDER
NDC Code 25543-012-03
Package Description: 1586 L in 1 CYLINDER
NDC Code 25543-012-04
Package Description: 4927 L in 1 CYLINDER
NDC Code 25543-012-05
Package Description: 7561 L in 1 CYLINDER
NDC Code 25543-012-06
Package Description: 13819 L in 1 CYLINDER
NDC Code 25543-012-07
Package Description: 15801 L in 1 CYLINDER
NDC Code 25543-012-08
Package Description: 18576 L in 1 CYLINDER
NDC Code 25543-012-09
Package Description: 95145 L in 1 CYLINDER
Product Details
What is NDC 25543-012?
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".