MedPath

Oxygen

Oxygen, Refrigerated Liquid USP

Approved
Approval ID

a200525a-06bf-485e-a61f-d78398a8ad38

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Feb 9, 2010

Manufacturers
FDA

Centrad Healthcare, LLC

DUNS: 868419446

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 Code50093-001
Product Classification
G
Generic Name
Oxygen
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
FDA Product Classification

INGREDIENTS (1)

OxygenActive
Quantity: 995 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