Label: FATAL-PLUS POWDER - pentobarbital sodium injection, solution

  • NDC Code(s): 0298-9372-68
  • Packager: Vortech Pharmaceuticals, Ltd.
  • Category: PRESCRIPTION ANIMAL DRUG LABEL
  • DEA Schedule: CII
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated December 21, 2016

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  • Description

    Fatal-Plus Powder

    Pentobarbital Sodium - 98 grams

    FOR VETERINARY USE ONLY

    For Euthanasia of Animals

    DIRECTIONS FOR MIXING:

    Slowly add water (150 mL to 200 mL).

    Replace cap and shake well until powder is dissolved.

    Add more water to the 250 mL mark only.

    Do not exceed the fill line (250 mL).

    DOSAGE AND ADMINISTRATION:

    Intravenous injection is the preferred route.  However, intraperitoneal or intracardiac injections may be made where the intravenous injection is impractical, as in the very small dog and cat, or in the comatose animal with depressed vascular function.  Inject rapidly 1 mL for every 10 lbs. body weight  Minimum 1 mL.

    WARNING:  Must not be used for therapeutic purposes.  Do not use in animals intended for food.
    ENVIRONMENTAL HAZARD:

    This product is toxic to wildlife.  Birds and mammals feeding on treated animals may be killed.  Birds and mammals feeding on treated animals may be killed.  Euthanized animals must be properly disposed of by deep burial, incineration, or other method in compliance with state and local laws, to prevent consumption of carcass material by scavenging wildlife.

    CAUTION:  Federal law restricts this drug to use by or on the order of a licensed veterinarian.

    POISON:  KEEP OUT OF THE REACH OF CHILDREN

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  • Principle Display Panel

    Fatal-Plus Powder - NDC: 0298-9372-68

    Pentobarbital Sodium - 98 grams

    FOR VETERINARY USE ONLY

    For Euthanasia of Animals

    DIRECTIONS FOR MIXING:

    Slowly add water (150 mL to 200 mL).

    Replace cap and shake well until powder is dissolved.

    Add more water to the 250 mL mark only.

    Do not exceed the fill line (250 mL).

    DOSAGE AND ADMINISTRATION:

    Intravenous injection is the preferred route.  However, intraperitoneal or intracardiac injections may be made where the intravenous injection is impractical, as in the very small dog and cat, or in the comatose animal with depressed vascular function.  Inject rapidly 1 mL for every 10 lbs. body weight  Minimum 1 mL.

    WARNING:  Must not be used for therapeutic purposes.  Do not use in animals intended for food.

    ENVIRONMENTAL HAZARD:

    This product is toxic to wildlife.  Birds and mammals feeding on treated animals may be killed.  Birds and mammals feeding on treated animals may be killed.  Euthanized animals must be properly disposed of by deep burial, incineration, or other method in compliance with state and local laws, to prevent consumption of carcass material by scavenging wildlife.

    CAUTION:  Federal law restricts this drug to use by or on the order of a licensed veterinarian.

    POISON: 

    KEEP OUT OF THE REACH OF CHILDREN
    powder

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  • INGREDIENTS AND APPEARANCE
    FATAL-PLUS POWDER  
    pentobarbital sodium injection, solution
    Product Information
    Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:0298-9372
    Route of Administration INTRAVENOUS, INTRAPERITONEAL, INTRACARDIAC DEA Schedule CII    
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Pentobarbital Sodium (UNII: NJJ0475N0S) (Pentobarbital - UNII:I4744080IR) Pentobarbital Sodium 392 mg  in 1 mL
    Product Characteristics
    Color blue (DARK BLUE) Score     
    Shape Size
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0298-9372-68 250 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 06/14/1982
    Labeler - Vortech Pharmaceuticals, Ltd. (052399276)
    Registrant - Vortech Pharmaceuticals, Ltd. (052399276)
    Establishment
    Name Address ID/FEI Business Operations
    Vortech Pharmaceuticals, Ltd 052399276 manufacture
    Establishment
    Name Address ID/FEI Business Operations
    Siegfried USA, LLC 001213784 api manufacture
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