NDC 14961-001 Oxygen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 14961-001-01
Package Description: 37 L in 1 CYLINDER
NDC Code 14961-001-02
Package Description: 103 L in 1 CYLINDER
NDC Code 14961-001-03
Package Description: 150 L in 1 CYLINDER
NDC Code 14961-001-04
Package Description: 171 L in 1 CYLINDER
NDC Code 14961-001-05
Package Description: 210 L in 1 CYLINDER
NDC Code 14961-001-06
Package Description: 248 L in 1 CYLINDER
NDC Code 14961-001-07
Package Description: 415 L in 1 CYLINDER
NDC Code 14961-001-08
Package Description: 588 L in 1 CYLINDER
NDC Code 14961-001-09
Package Description: 682 L in 1 CYLINDER
NDC Code 14961-001-10
Package Description: 1724 L in 1 CYLINDER
NDC Code 14961-001-11
Package Description: 3452 L in 1 CYLINDER
NDC Code 14961-001-12
Package Description: 7507 L in 1 CYLINDER
NDC Code 14961-001-13
Package Description: 212 L in 1 CYLINDER
NDC Code 14961-001-14
Package Description: 424 L in 1 CYLINDER
NDC Code 14961-001-15
Package Description: 691 L in 1 CYLINDER
NDC Code 14961-001-16
Package Description: 2678 L in 1 CYLINDER
NDC Code 14961-001-17
Package Description: 3606 L in 1 CYLINDER
NDC Code 14961-001-18
Package Description: 6999 L in 1 CYLINDER
NDC Code 14961-001-19
Package Description: 9427 L in 1 CYLINDER
Product Details
What is NDC 14961-001?
Which are Oxygen UNII Codes?
The UNII codes for the active ingredients in this product are:
- OXYGEN (UNII: S88TT14065)
- OXYGEN (UNII: S88TT14065) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Oxygen?
- RxCUI: 312172 - oxygen 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".