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Nitrous Oxide

nitrous oxide

Approved
Approval ID

a6f744e1-d94d-49e1-ab9f-9a88f04f5499

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Nov 16, 2023

Manufacturers
FDA

NEXAIR, LLC

DUNS: 927024422

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 Code12213-593
Application NumberNDA206009
Product Classification
M
Marketing Category
C73594
G
Generic Name
Nitrous Oxide
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateNovember 16, 2023
FDA Product Classification

INGREDIENTS (1)

NITROUS OXIDEActive
Quantity: 990 mL in 1 L
Code: K50XQU1029
Classification: ACTIB

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Nitrous Oxide - FDA Drug Approval Details