MedPath

OXYGEN

Liquid Oxygen

Approved
Approval ID

8c078dbb-8cd3-4b12-8695-80afde2e3b3b

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jun 17, 2010

Manufacturers
FDA

AIRWAY OXYGEN INC

DUNS: 052495116

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 Code59714-101
Product Classification
G
Generic Name
OXYGEN
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateJune 17, 2010
FDA Product Classification

INGREDIENTS (1)

OXYGENActive
Quantity: 99 L in 100 L
Code: S88TT14065
Classification: ACTIB

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OXYGEN - FDA Drug Approval Details