Nitrous Oxide
nitrous oxide
Approved
Approval ID
bd405eab-ac43-4590-975d-d0d1e8f78833
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 17, 2023
Manufacturers
FDA
Aero All Gas Company
DUNS: 004532065
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 Code10014-003
Application NumberNDA206009
Product Classification
M
Marketing Category
C73594
G
Generic Name
Nitrous Oxide
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateOctober 17, 2023
FDA Product Classification
INGREDIENTS (1)
NITROUS OXIDEActive
Quantity: 990 mL in 1 L
Code: K50XQU1029
Classification: ACTIB