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 July 27, 2017

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

View All Sections
  • INDICATIONS & USAGE

    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

    VED Epinephrine

  • INGREDIENTS AND APPEARANCE
    EPINEPHRINE 
    epinephrine injection
    Product Information
    Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:50989-102
    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:50989-102-1150 mL in 1 VIAL
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/12/2014
    Labeler - Vedco, Inc. (021634266)
View All Sections

Find additional resources

(also available in the left menu)

Safety

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

Related Resources

Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!