Oxygen

Oxygen

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

Company

DUNS: 079372105

Effective Date

October 20, 2023

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Oxygen(99 L in 100 L)

Manufacturing Establishments1

FDA-registered manufacturing facilities and establishments involved in the production, packaging, or distribution of this drug product.

Labeler

One Home Medical Equipment, LLC

DUNS Number

079372105

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

NDC Product Code

73266-001

Route of Administration

RESPIRATORY (INHALATION)

Effective Date

October 20, 2023

Ingredients

Code: S88TT14065Class: ACTIBQuantity: 99 L in 100 L