Label: NITROUS OXIDE- nitrous oxide gas

  • NDC Code(s): 72343-001-01
  • Packager: Nitrous Oxide of Canada
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated October 1, 2018

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  • PRINCIPAL DISPLAY PANEL

    Airgas

    2201

    Nitrous Oxide

    Refrigerated Liquid nitrous oxide

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  • INGREDIENTS AND APPEARANCE
    NITROUS OXIDE 
    nitrous oxide gas
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72343-001
    Route of Administration RESPIRATORY (INHALATION)
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    NITROUS OXIDE (UNII: K50XQU1029) (NITROUS OXIDE - UNII:K50XQU1029) NITROUS OXIDE 900 mL  in 1 L
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:72343-001-01 89936 L in 1 CYLINDER; Type 0: Not a Combination Product 01/01/2000
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA206009 01/01/2000
    Labeler - Nitrous Oxide of Canada (205078801)
    Registrant - Nitrous Oxide of Canada (205078801)
    Establishment
    Name Address ID/FEI Business Operations
    Nitrous Oxide of Canada 205078801 manufacture(72343-001)
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