Nitrous Oxide
Nitrous Oxide Label
Approved
Approval ID
d676898d-c455-44c6-83b7-d5f19d10264b
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 18, 2023
Manufacturers
FDA
MEDICAL-TECHNICAL GASES, INC.
DUNS: 019481373
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
NDC Product Code10736-017
Application NumberNDA209989
Marketing CategoryC73594
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateOctober 18, 2023
Generic NameNitrous Oxide
INGREDIENTS (1)
NITROUS OXIDEActive
Quantity: 995 mL in 1 L
Code: K50XQU1029
Classification: ACTIB