MedPath

Oxygen

Liquid Oxygen Label

Approved
Approval ID

65747dad-6c07-4b50-91c9-fcf37599741d

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Feb 19, 2010

Manufacturers
FDA

American Welding & Gas

DUNS: 035216530

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 Code49778-002
Product Classification
G
Generic Name
Oxygen
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateFebruary 19, 2010
FDA Product Classification

INGREDIENTS (1)

OxygenActive
Quantity: 992 L in 1000 L
Code: S88TT14065
Classification: ACTIB

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Oxygen - FDA Drug Approval Details