MedPath

Oxygen

Oxygen Shoulder Label

Approved
Approval ID

b3f8ad47-ab66-4b8e-b83f-0b6bcfa9c40c

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jul 30, 2010

Manufacturers
FDA

DENISON INC

DUNS: 031240120

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 Code24913-2234
Product Classification
G
Generic Name
Oxygen
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateJuly 30, 2010
FDA Product Classification

INGREDIENTS (1)

OXYGENActive
Quantity: 990 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