Label: BUPRENORPHINE solution

  • NDC Code(s): 70022-004-10
  • Packager: PAYLESS COMPOUNDERS, LLC
  • Category: ANIMAL COMPOUNDED DRUG
  • DEA Schedule: CIII
  • Marketing Status: unapproved drug other

Drug Label Information

Updated October 21, 2015

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  • PRINCIPAL DISPLAY PANEL

    buprenorphine inj MDV 0.6mg/mL
  • INGREDIENTS AND APPEARANCE
    BUPRENORPHINE 
    buprenorphine solution
    Product Information
    Product TypeANIMAL COMPOUNDED DRUGItem Code (Source)NDC:70022-004
    Route of AdministrationINTRAMUSCULAR, SUBCUTANEOUSDEA ScheduleCIII    
    Reporting Period20151006-20160405
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BUPRENORPHINE HYDROCHLORIDE (UNII: 56W8MW3EN1) (BUPRENORPHINE - UNII:40D3SCR4GZ) BUPRENORPHINE0.6 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    MANNITOL (UNII: 3OWL53L36A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70022-004-1010 mL in 1 VIAL, MULTI-DOSE; Number of Units = 10
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/06/2015
    Labeler - PAYLESS COMPOUNDERS, LLC (031728341)
    Establishment
    NameAddressID/FEIBusiness Operations
    PAYLESS COMPOUNDERS, LLC604160239outsourcing animal drug compounding
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