MedPath

Oxygen

Oxygen

Approved
Approval ID

e648bc38-2784-44f6-8788-3c69dcf69c1a

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Nov 18, 2009

Manufacturers
FDA

THH Acquisition LLC I dba Total Home Health

DUNS: 168725229

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 Code62789-0001
Product Classification
G
Generic Name
Oxygen
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateOctober 27, 2009
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