MedPath

OXYGEN

Approved
Approval ID

fefe2079-2105-40e8-8ae4-4d0465675335

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jan 1, 2010

Manufacturers
FDA

Capweld Inc

DUNS: 033340977

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 Code52849-100
Product Classification
G
Generic Name
OXYGEN
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateJanuary 1, 2010
FDA Product Classification

INGREDIENTS (1)

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

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