MedPath

Oxygen

Oxygen

Approved
Approval ID

4ab3fd7d-894b-4d60-abd9-f1e39efb0843

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jul 19, 2010

Manufacturers
FDA

Oxygen Plus

DUNS: 136760852

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 Code67777-001
Product Classification
G
Generic Name
Oxygen
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateJuly 19, 2010
FDA Product Classification

INGREDIENTS (1)

OxygenActive
Quantity: 99 L in 100 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