MedPath

OXYGEN

Approved
Approval ID

49d5a0eb-14ac-412e-a9d8-ed92488c643f

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Nov 8, 2023

Manufacturers
FDA

NLR Welding Supply, Inc.

DUNS: 144730421

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 Code62045-4333
Application NumberNDA205865
Product Classification
M
Marketing Category
C73594
G
Generic Name
OXYGEN
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateFebruary 9, 2018
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