Oxygen
Oxygen, Liquid USP-002
Approved
Approval ID
fd99ef4b-8a77-455d-b2a6-9a0d19a7b1fe
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 16, 2023
Manufacturers
FDA
Roberts Oxygen Company, Inc.
DUNS: 042646877
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 Code46123-002
Application NumberNDA205849
Product Classification
M
Marketing Category
C73594
G
Generic Name
Oxygen
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateNovember 16, 2023
FDA Product Classification
INGREDIENTS (1)
OXYGENActive
Quantity: 990 mL in 1 L
Code: S88TT14065
Classification: ACTIB