Oxygen
Oxygen
Approved
Approval ID
b8a4f8fa-2c11-4ee4-850d-d1ee80fb0000
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 18, 2023
Manufacturers
FDA
HARTMAN BROTHERS, INC.
DUNS: 032122699
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 Code49204-001
Application NumberNDA205712
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: 990 mL in 1 L
Code: S88TT14065
Classification: ACTIB