OXYGEN
OXYGEN
Approved
Approval ID
7a4aa7ab-08a4-4e93-90d7-5329b0e1a61b
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 18, 2023
Manufacturers
FDA
CEE-KAY SUPPLY, INC.
DUNS: 031018146
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 Code10218-001
Application NumberNDA205767
Product Classification
M
Marketing Category
C73594
G
Generic Name
OXYGEN
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateOctober 18, 2023
FDA Product Classification
INGREDIENTS (1)
OXYGENActive
Quantity: 995 mL in 1 L
Code: S88TT14065
Classification: ACTIB