Label: EPINEPHRINE injection

  • NDC Code(s): 58005-004-02
  • Packager: Sparhawk Laboratories, Inc.
  • Category: PRESCRIPTION ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated May 25, 2022

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  • INDICATIONS & USAGE

    1 mg/mL

    STERILE MULTIPLE DOSE VIAL

    FOR ANIMAL USE ONLY

    KEEP OUT OF REACH OF CHILDREN

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

    INDICATIONS

    For emergency use only in treating anaphylactoid shock in sheep, swine, cattle, horses, dogs and cats.

  • DOSAGE AND ADMINISTRATION

    Dogs and Cats: 0.1 to 0.5 mL injected Intramuscularly or Subcutaneously.

    Cattle, Horses, Sheep and Swine: 1 mL per 100 lbs of body weight injected Intramuscularly or Subcutaneously.

  • WARNING

    Do not use this product if it's color is pinkish or darker than slightly yellow or if it contains a precipitate.

  • COMPOSITION

    Each mL of sterile aqueous solution contains:

    Epinephrine ....................... 1 mg

    Sodium Chloride ................  0.1%

    Benzyl Alcohol ..................  1.5%

    Disodium Edetate, Sodium Metabisulfite, Hydrochloric Acid, and Water for Injection.



  • STORAGE AND HANDLING

    Store at controlled room temperature between 15° and 30°C (59° - 86°F).

    Protect from light.

    TAKE TIME OBSERVE LABEL DIRECTIONS

  • PRINCIPAL DISPLAY PANEL

    SLI Epinephrine

  • INGREDIENTS AND APPEARANCE
    EPINEPHRINE  
    epinephrine injection
    Product Information
    Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:58005-004
    Route of AdministrationINTRAMUSCULAR, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EPINEPHRINE (UNII: YKH834O4BH) (EPINEPHRINE - UNII:YKH834O4BH) EPINEPHRINE1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58005-004-0250 mL in 1 VIAL
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/23/2013
    Labeler - Sparhawk Laboratories, Inc. (147979082)
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Safety

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Clinical Trials, PubMed, Biochemical Data Summary

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