Label: BILOVET- tylosin injection, solution

  • NDC Code(s): 61133-4011-2, 61133-4011-3
  • Packager: Bimeda, Inc.
  • Category: PRESCRIPTION ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Animal Drug Application

Drug Label Information

Updated March 13, 2024

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

  • DESCRIPTION

    BiloVet®
    (tylosin injection)

    For Use in Cattle and Swine Only
    Use automatic syringe equipment only
    200 mg per mL
    An Antibiotic

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

  • INDICATIONS & USAGE

    INDICATIONS: In Beef Cattle and Non-lactating Dairy Cattle, BiloVet is indicated for use in the treatment of bovine respiratory complex (shipping fever, pneumonia) usually associated with Pasteurella multocida and Arcanobacterium pyogenes; foot rot (necrotic pododermatitis) and calf diphtheria caused by Fusobacterium necrophorum and metritis caused by Arcanobacterium pyogenes.

    In Swine, BiloVet is indicated for use in the treatment of swine arthritis caused by Mycoplasma hyosynoviae; swine pneumonia caused by Pasteurella spp.; swine erysipelas caused by Erysipelothrix rhusiopathiae; swine dysentery associated with Treponema hyodysenteriae when followed by appropriate medication in the drinking water and/or feed.

    Each mL contains 200 mg of tylosin activity (as tylosin base) in 50% propylene glycol with 4% benzyl alcohol, water for injection and hydrochloric acid for pH adjustment.

  • DOSAGE & ADMINISTRATION

    ADMINISTRATION AND DOSAGE: BiloVet is administered intramuscularly.

    Use automatic syringe equipment only

    BEEF CATTLE AND NON-LACTATING DAIRY CATTLE: Inject intramuscularly 8 mg per pound of body weight one time daily (1 mL per 25 pounds). Treatment should be continued 24 hours following remission of disease signs, not to exceed 5 days. Do not inject more than 10 mL per site.
    SWINE: Inject intramuscularly 4 mg per pound of body weight (1 mL per 50 pounds) twice daily. Treatment should be continued 24 hours following remission of disease signs, not to exceed 3 days. Do not inject more than 5 mL per site.
    Read accompanying directions fully before use.

    CAUTION: Do not mix BiloVet with other injectable solutions as this may cause a precipitation of the active ingredients.

  • WARNINGS

    WARNINGS:

    NOT FOR HUMAN USE.

    KEEP OUT OF REACH OF CHILDREN.

    Adverse reactions, including shock and death may result from overdosage in baby pigs.

    Do not attempt injection into pigs weighing less than 25 pounds (0.5 mL) with the common syringe. It is recommended that tylosin 50 mg/mL injection be used in pigs weighing less than 25 lbs.

    Do not administer to horses or other equines. Injection of tylosin in equines has been fatal.

    RESIDUE WARNING:

    Swine:

    Swine intended for human consumption must not be slaughtered within 14 days of the last use of this drug.

    RESIDUE WARNING:

    Cattle:

    Cattle intended for human consumption must not be slaughtered within 21 days of the last use of this drug product. This drug product is not approved for use in female dairy cattle 20 months of age or older, including dry dairy cows. Use in these cattle may cause drug residues in milk and/or in calves born to these cows. This product is not approved for use in calves intended to be processed for veal. A withdrawal period has not been established in pre-ruminating calves.

    If tylosin medicated drinking water is used as a follow-up treatment for swine dysentery, the animal should thereafter receive feed containing 40 to 100 grams of tylosin per ton for 2 weeks to assure depletion of tissue residues.

  • STORAGE AND HANDLING

    STORE AT 20°C-25°C (68°F -77°F).  Use within 28 days of first puncture and puncture a maximum of 5 times with automatic syringe equipment. When using a draw-off spike or needle larger than 4-gauge, discard any product remaining in the vial immediately after use.

  • SPL UNCLASSIFIED SECTION

    Approved by FDA under ANADA # 200-508

    To report suspected adverse drug events, for technical assistance or to obtain a copy of the Safety Data Sheet (SDS), contact Bimeda, Inc. at 1-888-524-6332. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS, or www.fda.gov/reportanimalae.

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    BILOVET 
    tylosin injection, solution
    Product Information
    Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:61133-4011
    Route of AdministrationINTRAMUSCULAR
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TYLOSIN (UNII: YEF4JXN031) (TYLOSIN - UNII:YEF4JXN031) TYLOSIN200 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    water (UNII: 059QF0KO0R)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61133-4011-2250 mL in 1 BOTTLE, GLASS
    2NDC:61133-4011-3500 mL in 1 BOTTLE, GLASS
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANADAANADA20050806/30/2021
    Labeler - Bimeda, Inc. (060492923)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bimeda- MTC256232216manufacture
    Establishment
    NameAddressID/FEIBusiness Operations
    Biovet645015512api manufacture
    Establishment
    NameAddressID/FEIBusiness Operations
    Shandong Lukang Shelile Pharmaceutical Co. Ltd.554404761api manufacture