MedPath

Oxygen

oxygen

Approved
Approval ID

61d0cf43-faef-2c08-e053-2a91aa0a6d62

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Dec 21, 2018

Manufacturers
FDA

J & M CYLINDER GASES, INC.

DUNS: 006977941

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 Code63862-001
Application NumberNDA205865
Product Classification
M
Marketing Category
C73594
G
Generic Name
Oxygen
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateDecember 21, 2018
FDA Product Classification

INGREDIENTS (1)

OXYGENActive
Quantity: 99.5 L in 1 L
Code: S88TT14065
Classification: ACTIB

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Oxygen - FDA Drug Approval Details