Label: POULTRYSULFA- sodium sulfamethazine sodium sulfamerazine sodium sulfaquinoxaline powder, for solution
- NDC Code(s): 23243-6764-1
- Packager: Huvepharma, Inc
- Category: PRESCRIPTION ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Animal Drug Application
Drug Label Information
Updated August 14, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- GENERAL PRECAUTIONS
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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
- STORAGE AND HANDLING
- SPL UNCLASSIFIED SECTION
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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.
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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
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Directions for Use:
PROPORTIONER SOLUTION (1 oz/gal) TANK MIX .04% Solution.025% Solution Add 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
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
POULTRYSULFA
sodium sulfamethazine sodium sulfamerazine sodium sulfaquinoxaline powder, for solutionProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:23243-6764 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFAMETHAZINE SODIUM (UNII: 7Z13P9Q95C) (SULFAMETHAZINE - UNII:48U51W007F) SULFAMETHAZINE SODIUM 78 g in 195 g SULFAMERAZINE SODIUM (UNII: JOV4UJY07O) (SULFAMERAZINE - UNII:UR1SAB295F) SULFAMERAZINE SODIUM 78 g in 195 g SULFAQUINOXALINE SODIUM (UNII: 21223EPJ40) (SULFAQUINOXALINE - UNII:WNW8115TM9) SULFAQUINOXALINE SODIUM 39 g in 195 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:23243-6764-1 40 in 1 PAIL 1 195 g in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NADA NADA100094 09/30/2016 Labeler - Huvepharma, Inc (619153559) Registrant - Huvepharma EOOD (552671651) Establishment Name Address ID/FEI Business Operations Huvepharma, Inc 883128204 manufacture, analysis, pack, label