NDC 55037-101 Oxygen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55037 - Matheson Tri-gas, Inc.
- 55037-101 - Oxygen
Product Packages
NDC Code 55037-101-21
Package Description: 38 L in 1 CYLINDER
NDC Code 55037-101-22
Package Description: 100 L in 1 CYLINDER
NDC Code 55037-101-23
Package Description: 160 L in 1 CYLINDER
NDC Code 55037-101-24
Package Description: 210 L in 1 CYLINDER
NDC Code 55037-101-25
Package Description: 250 L in 1 CYLINDER
NDC Code 55037-101-26
Package Description: 420 L in 1 CYLINDER
NDC Code 55037-101-27
Package Description: 480 L in 1 CYLINDER
NDC Code 55037-101-28
Package Description: 580 L in 1 CYLINDER
NDC Code 55037-101-29
Package Description: 630 L in 1 CYLINDER
NDC Code 55037-101-30
Package Description: 710 L in 1 CYLINDER
NDC Code 55037-101-31
Package Description: 680 L in 1 CYLINDER
NDC Code 55037-101-32
Package Description: 1100 L in 1 CYLINDER
NDC Code 55037-101-33
Package Description: 1700 L in 1 CYLINDER
NDC Code 55037-101-34
Package Description: 2100 L in 1 CYLINDER
NDC Code 55037-101-35
Package Description: 2500 L in 1 CYLINDER
NDC Code 55037-101-36
Package Description: 3400 L in 1 CYLINDER
NDC Code 55037-101-37
Package Description: 4400 L in 1 CYLINDER
NDC Code 55037-101-38
Package Description: 7000 L in 1 CYLINDER
NDC Code 55037-101-39
Package Description: 6300 L in 1 CYLINDER
NDC Code 55037-101-40
Package Description: 9600 L in 1 CYLINDER
NDC Code 55037-101-41
Package Description: 7200 L in 1 CYLINDER
NDC Code 55037-101-42
Package Description: 7800 L in 1 CYLINDER
NDC Code 55037-101-43
Package Description: 530 L in 1 CYLINDER
NDC Code 55037-101-44
Package Description: 2900 L in 1 CYLINDER
Product Details
What is NDC 55037-101?
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: 348831 - oxygen 99.2 % Gas for Inhalation
* 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".