Oxygen Refrigerated Liquid
Oxygen Refrigerated Liquid-USP
Approved
Approval ID
a66ada71-a046-4e70-8cab-e46659722b5d
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 4, 2022
Manufacturers
FDA
Elliot Hospital of the City of Manchester DBA: Home Medical Equipment and Infusion Services of Manchester & Southern N.H.
DUNS: 064324994
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 Code61888-0202
Application NumberNDA206023
Product Classification
M
Marketing Category
C73594
G
Generic Name
OXYGEN
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateOctober 4, 2022
FDA Product Classification
INGREDIENTS (1)
OXYGENActive
Quantity: 0.99 kg in 1 kg
Code: S88TT14065
Classification: ACTIB
Drug Labeling Information
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
LOINC: 51945-4Updated: 1/2/2018
Package Labeling:
