Label: OXYTOCIN - oxytocin injection, solution

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

Drug Label Information

Updated 12/14

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  • INGREDIENTS AND APPEARANCE
    OXYTOCIN 
    oxytocin injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:52533-105
    Route of Administration INTRAVENOUS DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    OXYTOCIN (OXYTOCIN) OXYTOCIN 2 [USP'U]  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    SODIUM CHLORIDE 600 mg  in 100 mL
    SODIUM LACTATE 310 mg  in 100 mL
    POTASSIUM CHLORIDE 30 mg  in 100 mL
    CALCIUM CHLORIDE 20 mg  in 100 mL
    DEXTROSE MONOHYDRATE 5 g  in 100 mL
    Other Ingredients
    Ingredient Kind Ingredient Name Quantity
    May contain ACETIC ACID  
    May contain SODIUM HYDROXIDE  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:52533-105-44 1000 mL in 1 BAG
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 11/12/2012
    Labeler - Cantrell Drug Company (035545763)
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