MedPath

NITROUS OXIDE

Approved
Approval ID

421af5eb-9807-4fc9-8763-8b0057c0d5cf

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.

NITROUS OXIDE

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code52849-500
Product Classification
G
Generic Name
NITROUS OXIDE
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateJanuary 1, 2010
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