OXYGEN
Oxygen
Approved
Approval ID
aae8e8ff-f579-462e-bbb7-7d710313890c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 18, 2023
Manufacturers
FDA
MID-SOUTH WELDING SUPPLY, INC.
DUNS: 095705448
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 Code51400-001
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: 99 L in 100 L
Code: S88TT14065
Classification: ACTIB