MedPath

Oxygen

Approved
Approval ID

7629851e-ef8a-4900-8688-b94d37ea77ed

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Aug 11, 2011

Manufacturers
FDA

W. H. Goodale Co. Inc.

DUNS: 011203064

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 Code50597-010
Product Classification
G
Generic Name
oxygen
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateAugust 11, 2011
FDA Product Classification

INGREDIENTS (1)

OXYGENActive
Quantity: 210 mL in 1 L
Code: S88TT14065
Classification: ACTIB

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Oxygen - FDA Drug Approval Details