Animal NDC 23243-6764-1 Poultrysulfa

Sodium Sulfamethazine Sodium Sulfamerazine Sodium Sulfaquinoxaline

Animal Product Information

Field Name Field Value
Animal NDC Code 23243-6764-1
Proprietary Name Poultrysulfa What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name Sodium Sulfamethazine Sodium Sulfamerazine Sodium Sulfaquinoxaline What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Labeler Name Huvepharma, Inc
Product Type Prescription Animal Drug
Usage Information
    For Use in Drinking Water OnlyAs an aid in the control of coccidiosis and acute fowl cholera in chickens and acute fowl choleraand coccidiosis in turkeys, when caused by pathogens susceptible to sulfamerazine, sulfamethazine and sulfaquinoxaline.SOLUBLE POWDERFor Use in Chickens and TurkeysTHIS PACKET CONTAINS:78 grams Sodium Sulfamerazine Activity78 grams Sodium Sulfamethazine Activity39 grams Sodium Sulfaquinoxaline Activity
Active Ingredient(s)
  • Sulfamethazine Sodium
  • Sulfaquinoxaline Sodium
  • Sulfamerazine Sodium
Marketing Category NADA - NEW ANIMAL DRUG APPLICATION What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
FDA Application Number NADA100094 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Poultrysulfa Animal Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Other



PoultrySulfa®

(sulfamerazine, sulfamethazine and sulfaquinoxaline)

Antimicrobial
For Oral Veterinary Use Only

Restricted Drug (California) - Use only as directed.

Approved by FDA under NADA #100-094

P08-9001BF Rev. 01-2022


General Precautions



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

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.


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


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).


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.


* The information on this page is for an ANIMAL PRODUCT, please review the complete disclaimer below.