HELIUM
Approved
Approval ID
8c473d18-b656-4e00-8fbc-6e1128d41254
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Apr 27, 2011
Manufacturers
FDA
Acetylene Oxygen Company
DUNS: 008110181
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
HELIUM
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code10006-008
Product Classification
G
Generic Name
HELIUM
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateApril 27, 2011
FDA Product Classification
INGREDIENTS (1)
HELIUMActive
Quantity: 99 L in 100 L
Code: 206GF3GB41
Classification: ACTIB