OXYGEN
LIQUID OXYGEN LABEL AND LOT LABEL
Approved
Approval ID
083f7374-3eda-42a7-b3a3-ee5f5ee11359
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 26, 2009
Manufacturers
FDA
Medox Healthcare
DUNS: 116340592
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 Code65300-123
Product Classification
G
Generic Name
OXYGEN
Product Specifications
Route of AdministrationNASAL
Effective DateOctober 26, 2009
FDA Product Classification
INGREDIENTS (1)
OXYGENActive
Quantity: 210 mL in 1 L
Code: S88TT14065
Classification: ACTIB