Label: FLORCON- florfenicol solution, concentrate

  • NDC Code(s): 17033-425-22
  • Packager: Dechra Veterinary Products
  • Category: PRESCRIPTION ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Animal Drug Application

Drug Label Information

Updated May 9, 2023

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  • SPL UNCLASSIFIED SECTION

    FLORCON

    (florfenicol)

    An Antimicrobial 2.3% Concentrate Solution

    For Oral Use in Swine Drinking Water Only.

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

    Approved by FDA under ANADA #200-589

    For use in Animals Only

    IMPORTANT: See Product Information sheet for complete directions and warnings before using.

  • DESCRIPTION

    DESCRIPTION:FLORCON (florfenicol) Oral Concentrate is a synthetic broad-spectrum antibiotic. Each milliliter (mL) of FLORCON 2.3% Concentrate Solution contains 23 mg florfenicol.

  • INDICATIONS & USAGE

    INDICATIONS:  FLORCON 2.3% Concentrate Solution is indicated for the treatment of swine respiratory disease associated with Actinobacillus pleuropneumoniae, Pasteurella multocida, Salmonella choleraesuis, and Streptococcus suis in swine.

  • DOSAGE & ADMINISTRATION

    DOSAGE AND ADMINISTRATION:

    For Proportioner: To produce drinking water with a final concentration of 400 mg/gallon (100 ppm): Fill the bottle of FLORCON 2.3% Concentrate Solution with water to the fill line.  Add the contents of the bottle to the mixing tank. Mix thoroughly. Confirm that the proportioner is set to deliver 1:128 (0.8%).  Turn on the proportioner. Verify that the drinkers are operational.

    For Bulk Tank: To produce drinking water with a final concentration o f 400 mg/gallon (100 ppm): Add the FLORCON 2.3% Concentrate Solution to the drinking water in the bulk tank. Use one bottle of FLORCON 2.3% Concentrate Solution for every 128 gallons of water.

    The medicated water should be administered as the only source of drinking water for five (5) consecutive days. Medication should be initiated promptly when swine respiratory disease is diagnosed.

  • PRECAUTIONS

    PRECAUTIONS: Do not use this product at any other proportioner setting. This will result in precipitation of product. This product is not recommended for use in automatic water proportioners if water hardness is greater than 275 ppm. Water proportioners should be tested for accuracy before use. Do not use or store this product in galvanized metal watering systems or containers. Do not operate chlorinators while administering medication.

    Residue Warnings

  • WARNINGS

    WARNINGS:  This product contains material that can be irritating to skin and eyes. Avoid direct contact with skin, eyes, and clothes. In case of accidental eye exposure, flush with water for 15 minutes. In case of accidental skin exposure, wash with soap and water. Remove contaminated clothing. Consult a physician if irritation persists. The Safety Data Sheet (SDS) contains more detailed occupational safety information.

    NOT FOR HUMAN USE.     KEEP OUT OF REACH OF CHILDREN.

    CONTACT INFORMATION: To report suspected adverse drug events, for technical assistance or to obtain a copy of the Safety Data Sheet (SDS), contact Dechra Veterinary Products at 1-866-933-2472. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS or online at http://www.fda.gov/reportanimalae

  • PRECAUTIONS

    PRECAUTION:  The effects of FLORCON 2.3% Concentrate Solution on swine reproductive performance, pregnancy, and lactation have not been determined.  Do not use in swine intended for breeding.

  • ADVERSE REACTIONS

    ADVERSE REACTION: Perianal inflammation may occur transiently following treatment.

  • CLINICAL PHARMACOLOGY

    CLINICAL PHARMACOLOGY: Florfenicol is a bacteriostatic agent whose antimicrobial activity is linked to time above MIC.

    The pharmacokinetic disposition of FLORCON 2.3% Concentrate Solution was evaluated in swine following oral gavage dosing (15 mg/kg), intravenous (IV) dosing (15 mg/kg), and during a five (5) day course of ad libitum administration in drinking water (100 ppm) (Table 1).  Despite the rapid elimination seen after IV injection or oral gavage dosing, when administered in medicated drinking water, florfenicol concentrations in the serum of most swine were maintained well above 1.0 mcg/mL for the majority of the (5) day dosing interval. These results are consistent with product effectiveness when administered in drinking water concentrations of 100 ppm over a five (5) day dosing period.

    Although the extent of oral drug absorption (F) tended to be variable (24% to 97% following a single oral gavage dose), florfenicol was rapidly absorbed.  Its terminal elimination half-life (T1/2) was also rapid, ranging between two (2) to three (3) hours.

    The average systemic clearance (CLB) following IV administration was 5.6 mL/kg/min. Since the florfenicol steady state volume of distribution (VDSS) closely approximates that of total body water, peripheral tissue concentrations are expected to be similar to those concentrations observed in serum.

    Table 1. Pharmacokinetic Parameter Values of Florfenicol

    following IV or Gavage Dosing

    Parameter

    Mean Value (% CV)

    Vdssa (L/kg)

    0.95 (6)

    CLB(mL/kg/min)

    5.57 (11)

    T ½a (hrs)

    2.2 (14)

    Fb (%)

    24-97

    aparameter estimate based on intravenous data

    bparameter range based upon a single oral gavage dose

  • MICROBIOLOGY

    MICROBIOLOGY: Florfenicol is a synthetic broad-spectrum antibiotic active against many gram-negative and gram-positive bacteria isolated from domestic animals.  It acts by inhibiting bacterial protein synthesis.  In vivo and in vitro activity has been demonstrated against commonly isolated pathogens involved in swine respiratory disease including Actinobacillus pleuropneumoniae, Pasteurella multocida, Salmonella choleraesuis, and Streptococcus suis.

    The minimum inhibitory concentration (MIC) of florfenicol was determined for isolates obtained from natural respiratory infections of swine from  1990-2001 (Table 2).  Susceptibility testing followed the methods of the National Committee of Clinical Laboratory Standards.  Reference strains included Escherichia coli ATCC 25922 with a QC range of 2-8 mcg/mL and Actinobacillus pleuropneumoniae ATCC 27090 with a QC range of 0.25-1 mcg/mL.

    Table 2. MIC Values of Florfenicol Against

     Bacterial Isolates from Swine

    Organism

         Isolate

         Numbers

         MIC90 *

        (mcg/mL)

        MIC Range

        (mcg/mL)

    Actinobacillus

    pleuropneumoniae

         360

        0.50

        ≤0.125-2.0

    Pasteurella multocida

         335

        0.50

        ≤0.125-2.0

    Salmonella

    choleraesuis

         46

        4.0

        2.0-4.0

    Streptococcus suis

         203

        2.0

        0.5-2.0

    *The minimum inhibitory concentration for 90 % of the isolates

  • ANIMAL PHARMACOLOGY & OR TOXICOLOGY

    ANIMAL SAFETY: A target animal safety study was conducted to evaluate the tolerance and effects of florfenicol when orally administered to swine via the drinking water at a rate of 400, 1200, and 2000 mg/gal (1x, 3x, or 5x the clinical dose) for fifteen (15) to sixteen (16) consecutive days (3x the clinical duration), and at 4000 mg/gal (10x clinical dose) for five (5) to six (6) consecutive days (1x the clinical duration).  

    Transient treatment-related constipation and anal swelling were seen in the 3x, 5x, and 10x treatment groups.  The constipation in these groups was attributed in part to decreased water consumption during the medication period.  There was a decrease in weight gains for the 3x, 5x, and 10x treatment groups compared with the nonmedicated control group.  Transient treatment-related decreases in feed consumption were seen in the 3x, 5x, and 10x treatment groups compared with the nonmedicated control group.  Transient treatment-related decreases in water consumption were noted in all test article-treated groups (1x, 3x, 5x, and 10x) compared with the nonmedicated control group.

    The results show that FLORCON 2.3% Concentrate Solution can be safely administered to swine according to the recommended clinical regimen of 400 mg/gal in the drinking water for five (5) consecutive days. 

  • STORAGE AND HANDLING

    STORAGE CONDITIONS:  Store between 2°-25°C (36°-77°F).

  • HOW SUPPLIED

    HOW SUPPLIED: FLORCON 2.3% Concentrate Solution is supplied in one gallon plastic bottles with 2.2 liter fill.

    Manufactured for:
    Dechra Veterinary Products
    Overland Park, KS 66211

    Rev. May 2023

  • PRINCIPAL DISPLAY PANEL

    Dechra Florcon Container Label

  • INGREDIENTS AND APPEARANCE
    FLORCON 
    florfenicol solution, concentrate
    Product Information
    Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:17033-425
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FLORFENICOL (UNII: 9J97307Y1H) (FLORFENICOL - UNII:9J97307Y1H) FLORFENICOL23 mg  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17033-425-222200 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANADAANADA20058905/09/2023
    Labeler - Dechra Veterinary Products (362142734)
    Registrant - Med-Pharmex, Inc. (025353699)
    Establishment
    NameAddressID/FEIBusiness Operations
    Med-Pharmex, Inc.025353699manufacture