MedPath

Nitrous Oxide

Nitrous Oxide

Approved
Approval ID

8f0149cb-5f7f-4c6e-99ce-ceaaf3d99466

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jan 18, 2013

Manufacturers
FDA

Fullerton Welding Supply

DUNS: 556832384

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Nitrous Oxide

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code42751-1070
Product Classification
G
Generic Name
Nitrous Oxide
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateNovember 12, 2009
FDA Product Classification

INGREDIENTS (1)

NITROUS OXIDEActive
Quantity: 99 L in 100 L
Code: K50XQU1029
Classification: ACTIB

MedPath

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

© 2025 MedPath, Inc. All rights reserved.

Nitrous Oxide - FDA Drug Approval Details