Label: EPINEPHRINE injection

  • Category: PRESCRIPTION ANIMAL DRUG LABEL
  • DEA Schedule: None
  • 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 April 18, 2018

If you are a consumer or patient please visit this version.

  • 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)