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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code10736-017
Application NumberNDA209989
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