MedPath

Oxygen

Oxygen

Approved
Approval ID

937560e9-6f89-006a-e053-2995a90afb91

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Oct 22, 2019

Manufacturers
FDA

Timberlake Respiratory Care and Home Medical

DUNS: 011931215

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 Code54292-123
Product Classification
G
Generic Name
Oxygen
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateOctober 22, 2019
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