Nitrous Oxide
Nitrous Oxide Label
Approved
Approval ID
ffcfc7c1-5806-4f37-9a0f-f64cb06410e0
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 3, 2010
Manufacturers
FDA
Encompass Medical & Specialty Gases, Ltd.
DUNS: 963344143
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 Code48883-004
Product Classification
G
Generic Name
Nitrous Oxide
Product Specifications
Route of AdministrationRECTAL
Effective DateDecember 3, 2010
FDA Product Classification
INGREDIENTS (1)
Nitrous OxideActive
Quantity: 990 mL in 1 L
Code: K50XQU1029
Classification: ACTIB