MedPath

Oxygen

Approved
Approval ID

6522d8a4-2658-444d-8412-d2a2fe0532b3

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Nov 4, 2009

Manufacturers
FDA

Allen's Cylinder Testing & Inspection Company

DUNS: 005292460

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 Code49790-001
Product Classification
G
Generic Name
Oxygen
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateNovember 4, 2009
FDA Product Classification

INGREDIENTS (1)

OxygenActive
Quantity: 992 mL in 1 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