Label: MORPHINE SULFATE - morphine sulfate injection, solution

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: CII
  • Marketing Status: unapproved drug other

Drug Label Information

Updated 05/14

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  • INGREDIENTS AND APPEARANCE
    MORPHINE SULFATE 
    morphine sulfate injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-161
    Route of Administration INTRAVENOUS, INTRAMUSCULAR, INTRATHECAL, EPIDURAL DEA Schedule CII    
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Morphine Sulfate (UNII: X3P646A2J0) (Morphine - UNII:76I7G6D29C) Morphine Sulfate 2 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    Sodium Chloride (UNII: 451W47IQ8X) 9 mg  in 1 mL
    Water (UNII: 059QF0KO0R)  
    Other Ingredients
    Ingredient Kind Ingredient Name Quantity
    May contain SULFURIC ACID (UNII: O40UQP6WCF)  
    May contain SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:52533-161-45 1 mL in 1 SYRINGE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 02/22/2012
    Labeler - Cantrell Drug Company (035545763)
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