Label: MEPERIDINE HCL - meperidine hydrochloride injection, solution 

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

Drug Label Information

Updated 04/14

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  • INGREDIENTS AND APPEARANCE
    MEPERIDINE HCL 
    meperidine hcl injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:52533-042
    Route of Administration INTRAVENOUS DEA Schedule CII    
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MEPERIDINE HYDROCHLORIDE (MEPERIDINE) MEPERIDINE HYDROCHLORIDE 10 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    Sodium Chloride 9 mg  in 1 mL
    WATER  
    Other Ingredients
    Ingredient Kind Ingredient Name Quantity
    May contain HYDROCHLORIC ACID  
    May contain SODIUM HYDROXIDE  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:52533-042-04 50 mL in 1 SYRINGE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 01/23/2012
    Labeler - Cantrell Drug Company (035545763)
    Establishment
    Name Address ID/FEI Business Operations
    Cantrell Drug Company 035545763 manufacture(52533-042), human drug compounding outsourcing facility(52533-042)(No intent to compound 506E (drug shortage) drugs)(Not compounding from bulk ingredient)
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