MedPath

OXYGEN

Approved
Approval ID

e155c7de-8de4-41bb-8119-a1bae69bc052

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jan 1, 2010

Manufacturers
FDA

Hampton Homecare

DUNS: 112791962

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

OXYGEN

PRODUCT DETAILS

NDC Product Code65067-321
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateJanuary 1, 2010
Generic NameOXYGEN

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