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Nitrous Oxide

Nitrous Oxide

Approved
Approval ID

b76cb73a-46f4-48d5-9f8d-b0872f2cfe2b

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Oct 18, 2023

Manufacturers
FDA

General Air Service & Supply Co

DUNS: 051227338

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 Code21220-122
Application NumberNDA205704
Product Classification
M
Marketing Category
C73594
G
Generic Name
Nitrous Oxide
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateOctober 18, 2023
FDA Product Classification

INGREDIENTS (1)

NITROUS OXIDEActive
Quantity: 995 mL in 1 L
Code: K50XQU1029
Classification: ACTIB

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Nitrous Oxide - FDA Drug Approval Details