Oxygen
Oxygen, Liquid USP
Approved
Approval ID
968e6364-9659-4d31-b0b3-e715036195af
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 6, 2009
Manufacturers
FDA
Roberts Home Medical, Inc.
DUNS: 608714825
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 Code17134-001
Product Classification
G
Generic Name
Oxygen
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateNovember 6, 2009
FDA Product Classification
INGREDIENTS (1)
OxygenActive
Quantity: 990 mL in 1 L
Code: S88TT14065
Classification: ACTIB