Label: POULTRYSULFA- sodium sulfamethazine sodium sulfamerazine sodium sulfaquinoxaline powder, for solution

  • Category: PRESCRIPTION ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Animal Drug Application

Drug Label Information

Updated August 14, 2023

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

  • SPL UNCLASSIFIED SECTION

    PoultrySulfa®

    (sulfamerazine, sulfamethazine and sulfaquinoxaline)

    Antimicrobial
    For Oral Veterinary Use Only

  • GENERAL PRECAUTIONS

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

  • INDICATIONS & USAGE

    For Use in Drinking Water Only

    As an aid in the control of coccidiosis and acute fowl cholera in chickens and acute fowl cholera
    and coccidiosis in turkeys, when caused by pathogens susceptible to sulfamerazine, sulfamethazine 
    and sulfaquinoxaline.

    SOLUBLE POWDER

    For Use in Chickens and Turkeys

    THIS PACKET CONTAINS:
    78 grams Sodium Sulfamerazine Activity
    78 grams Sodium Sulfamethazine Activity
    39 grams Sodium Sulfaquinoxaline Activity

  • GENERAL PRECAUTIONS

    CAUTION:

    Not for use in humans. Keep out of reach of children. Federal law prohibits the extralabel use of 
    this product in lactating dairy cattle.

  • STORAGE AND HANDLING

    HUVEPHARMA®

    Manufactured for:
    Huvepharma, Inc
    525 Westpark Drive, Suite 230
    Peachtree City, GA 30269

    Store between 20°C - 25°C
    (68°F- 77°F) with excusions permitted
    between 15°C - 40°C (59°F - 104°F).

  • SPL UNCLASSIFIED SECTION

    Take Time

    Restricted Drug (California) - Use only as directed.

    Approved by FDA under NADA #100-094

    P08-9001BF Rev. 01-2022

  • ADVERSE REACTIONS

    To report suspected adverse drug events, for technical assistance or to obtain a copy of the
    Safety Data Sheet (SDS), contact Huvepharma, Inc. at 1-877-994-4883 or www.huvepharma.us.
    For additional information about adverse drug experience reporting for animal drugs, contact
    FDA at 1-888-FDA-VETS or http://www.fda.gov/reportanimalae.

    HUVEPHARMA and PoultrySulfa are registered trademarks of Huvepharma EOOD.

  • VETERINARY INDICATIONS

    DIRECTIONS

    Acute Fowl Cholera - TURKEYS AND  CHICKENS: As an aid in the control
    of acute fowl cholera caused by Pasteurella multocida susceptible to
    sulfamerazine, sulfamethazine and  sulfaquinoxaline. Provide medicated
    water (.04% solution) for 2-3 days. If disease recurs, repeat treatment.

    Coccidiosis - TURKEYS: As an aid in the control of coccidiosis caused by Eimeria
    meleagrimitis and E. adenoeides susceptible to sulfamerazine, sulfamethazine
    and sulfaquinoxaline. Provide medicated water (.025% solution) for 2 days, then
    plain water for 3 days, then medicated water (.025% solution) for 2 days,
    then plain water for 3 days, then medicated water (.025% solution) for 2 days.
    Repeat if necessary. DO NOT CHANGE LITTER.

    Coccidiosis - CHICKENS: As an aid in the control of coccidiosis caused by Eimeria
    tenella and E. necatrix susceptible to sulfamerazine, sulfamethazine and
    sulfaquinoxaline. Provide medicated water (.04% solution) for 2-3 days, then plain
    water for 3 days, then medicated water (.025% solution) for 2 days. If bloody
    droppings appear, repeat at .025% level for 2 more days. DO NOT CHANGE LITTER.

    PoultrySulfa®
    (sulfamerazine, sulfamethazine and sulfaquinoxaline)

  • WARNINGS

                                     Warning (Human Food)

    Do not treat chickens or turkeys within 14 days of slaughter for food.
    Do not medicate chickens or turkeys producing eggs for human consumption.

  • Directions for Use:

     PROPORTIONER SOLUTION (1 oz/gal)               TANK MIX
     .04% Solution.025% SolutionAdd one pack to 1 gallon (3.8 liters)
    Add one pack to 1.6 gallons (6.1 liters)
    Add one pack to 128 gallonsAdd one pack to 206 gallons

    MAKE FRESH SOLUTION DAILY. If improvement is not noted in 72 hours, consult your veterinarian.
    During treatment use only medicated water unless otherwise directed. For control of disease outbreaks
    medication should be initiated as soon as diagnosis is determined. Treated animals must actually
    consume enough medicated water to provide a therapeutic dose. Do not mix or administer in
    galvanized containers. Dispose of any waste or unused portions properly.

  • PRECAUTIONS

    PRECAUTION: May cause toxic reactions unless drug is evenly mixed in water at dosages indicated and used
    according to label directions.

  • PRINCIPAL DISPLAY PANEL

    Bag Label Image

  • INGREDIENTS AND APPEARANCE
    POULTRYSULFA 
    sodium sulfamethazine sodium sulfamerazine sodium sulfaquinoxaline powder, for solution
    Product Information
    Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:23243-6764
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFAMETHAZINE SODIUM (UNII: 7Z13P9Q95C) (SULFAMETHAZINE - UNII:48U51W007F) SULFAMETHAZINE SODIUM78 g  in 195 g
    SULFAMERAZINE SODIUM (UNII: JOV4UJY07O) (SULFAMERAZINE - UNII:UR1SAB295F) SULFAMERAZINE SODIUM78 g  in 195 g
    SULFAQUINOXALINE SODIUM (UNII: 21223EPJ40) (SULFAQUINOXALINE - UNII:WNW8115TM9) SULFAQUINOXALINE SODIUM39 g  in 195 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:23243-6764-140 in 1 PAIL
    1195 g in 1 PACKET
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NADANADA10009409/30/2016
    Labeler - Huvepharma, Inc (619153559)
    Registrant - Huvepharma EOOD (552671651)
    Establishment
    NameAddressID/FEIBusiness Operations
    Huvepharma, Inc883128204manufacture, analysis, pack, label