Oxygen
Liquid Oxygen USP Canada
Approved
Approval ID
ae2013c3-a153-4eb3-9168-01d0b5df7ad0
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 5, 2023
Manufacturers
FDA
Linde Canada Inc.
DUNS: 201774676
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Oxygen
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code49479-722
Application NumberNDA205986
Product Classification
M
Marketing Category
C73594
G
Generic Name
Oxygen
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateDecember 5, 2023
FDA Product Classification
INGREDIENTS (1)
OXYGENActive
Quantity: 990 mL in 1 L
Code: S88TT14065
Classification: ACTIB