Label: EPINEPHRINE injection

  • Category: PRESCRIPTION ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated April 18, 2018

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  • INDICATIONS & USAGE

    STERILE MULTIPLE DOSE VIAL

    FOR USE IN ANIMALS 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, 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 its color is pinkish or darker than slightly yellow or 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 15o and 30o (59o - 86oF).

    Protect from light.

  • PRINCIPAL DISPLAY PANEL

    V1-Epinephrine-18

  • INGREDIENTS AND APPEARANCE
    EPINEPHRINE 
    epinephrine injection
    Product Information
    Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:13985-532
    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:13985-532-5050 mL in 1 VIAL
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/07/2012
    Labeler - MWI/VetOne (019926120)
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Safety

Report Adverse Events (Animal Drug), FDA Safety Recalls (Animal Drug)

Related Resources

Clinical Trials, PubMed, Biochemical Data Summary

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