NDC 61519-001 Oxygen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 61519-001-01
Package Description: 113 L in 1 CYLINDER
NDC Code 61519-001-02
Package Description: 170 L in 1 CYLINDER
NDC Code 61519-001-03
Package Description: 255 L in 1 CYLINDER
NDC Code 61519-001-04
Package Description: 45 L in 1 CYLINDER
NDC Code 61519-001-05
Package Description: 680 L in 1 CYLINDER
NDC Code 61519-001-06
Package Description: 2167 L in 1 CYLINDER
NDC Code 61519-001-07
Package Description: 906 L in 1 CYLINDER
NDC Code 61519-001-08
Package Description: 566 L in 1 CYLINDER
NDC Code 61519-001-09
Package Description: 340 L in 1 CYLINDER
NDC Code 61519-001-10
Package Description: 221 L in 1 CYLINDER
NDC Code 61519-001-11
Package Description: 212 L in 1 CYLINDER
NDC Code 61519-001-12
Package Description: 7503 L in 1 CYLINDER
NDC Code 61519-001-13
Package Description: 4248 L in 1 CYLINDER
NDC Code 61519-001-14
Package Description: 3455 L in 1 CYLINDER
NDC Code 61519-001-15
Package Description: 2549 L in 1 CYLINDER
NDC Code 61519-001-16
Package Description: 1699 L in 1 CYLINDER
NDC Code 61519-001-17
Package Description: 623 L in 1 CYLINDER
NDC Code 61519-001-18
Package Description: 425 L in 1 CYLINDER
NDC Code 61519-001-19
Package Description: 198 L in 1 CYLINDER
Product Details
What is NDC 61519-001?
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".