Nitrous Oxide
NITROUS OXIDE, REFRIGERATED LIQUID LABEL
Approved
Approval ID
500cd52e-9300-4a8a-b043-15e419f68641
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 22, 2011
Manufacturers
FDA
Welding & Therapy Service Inc.
DUNS: 056823511
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 Code33344-004
Product Classification
G
Generic Name
Nitrous Oxide
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateJuly 22, 2011
FDA Product Classification
INGREDIENTS (1)
Nitrous OxideActive
Quantity: 99 L in 100 L
Code: K50XQU1029
Classification: ACTIB