NDC 48883-007 Helium Oxygen Mix
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 48883-007-01
Package Description: 617 L in 1 CYLINDER
NDC Code 48883-007-02
Package Description: 623 L in 1 CYLINDER
NDC Code 48883-007-03
Package Description: 629 L in 1 CYLINDER
NDC Code 48883-007-04
Package Description: 640 L in 1 CYLINDER
NDC Code 48883-007-05
Package Description: 654 L in 1 CYLINDER
NDC Code 48883-007-06
Package Description: 5689 L in 1 CYLINDER
NDC Code 48883-007-07
Package Description: 5743 L in 1 CYLINDER
NDC Code 48883-007-08
Package Description: 5796 L in 1 CYLINDER
NDC Code 48883-007-09
Package Description: 5904 L in 1 CYLINDER
NDC Code 48883-007-10
Package Description: 6009 L in 1 CYLINDER
Product Details
What is NDC 48883-007?
Which are Helium Oxygen Mix UNII Codes?
The UNII codes for the active ingredients in this product are:
- HELIUM (UNII: 206GF3GB41)
- HELIUM (UNII: 206GF3GB41) (Active Moiety)
- OXYGEN (UNII: S88TT14065)
- OXYGEN (UNII: S88TT14065) (Active Moiety)
* Please review the disclaimer below.
[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".