POULTRY SULFA- sodium sulfamethazine sodium sulfamerazine sodium sulfaquinoxaline powder, for solution

PoultrySulfa by

Drug Labeling and Warnings

PoultrySulfa by is a Animal medication manufactured, distributed, or labeled by Huvepharma, Inc, Huvepharma EOOD, Huvepharma, Inc - Longmont. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Front Panel

PoultrySulfa®

(sulfamerazine, sulfamethazine and sulfaquinoxaline)

Antimicrobial
For Oral Veterinary Use Only

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

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

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.

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

Restricted Drug (California) - Use only as directed.

NADA 100-094, Approved by FDA

To report adverse effects, access medical informaiton, or obtain

additional product information, call 1-877-426-7768

Huvepharma and PoultrySulfa are registered trademarks fo Huvepharma EOOD.

Huvepharma:

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

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.

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

Directions for Use:

PROPORTIONER SOLUTION (1 oz/gal) - TANK MIX
.04% Solution Add one pack to 1 gallon (3.8 liters) - Add one pack to 128 gallons
.025% Solution Add one pack to 1.6 gallons (6.1 liters) - Add 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 ingalvanized containers. Dispose of any waste or unused portions
properly.

Precaution

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

SPL UNCLASSIFIED SECTION

PoultrySulfa®
(sulfamerazine, sulfamethazine and sulfaquinoxaline)

Bag Label Image

Bag Label Image

INGREDIENTS AND APPEARANCE

POULTRY SULFA 
sodium sulfamethazine sodium sulfamerazine sodium sulfaquinoxaline powder, for solution

Product Information
Product Type	OTC 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	0.4 g  in 1 g
SULFAMERAZINE SODIUM (UNII: JOV4UJY07O) (SULFAMERAZINE - UNII:UR1SAB295F)	SULFAMERAZINE SODIUM	0.4 g  in 1 g
SULFAQUINOXALINE SODIUM (UNII: 21223EPJ40) (SULFAQUINOXALINE - UNII:WNW8115TM9)	SULFAQUINOXALINE SODIUM	0.4 g  in 1 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 (619153559)

Registrant - Huvepharma EOOD (552691651)

Establishment
Name	Address	ID/FEI	Business Operations
Huvepharma, Inc - Longmont		080346321	manufacture, analysis, pack, label

Establishment
Name	Address	ID/FEI	Business Operations
SHANGHAI ZHONGXI SUNVE PHARMACEUTICAL CO., LTD.		544646342	api manufacture