Animal NDC 23243-6771-2 Sul-q-nox
Sulfaquinoxaline
Animal Product Information
| Field Name | Field Value |
|---|---|
| Animal NDC Code | 23243-6771-2 |
| Proprietary Name | Sul-q-nox 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 | 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 |
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| Active Ingredient(s) |
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| 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 | NADA006891 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. |
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Sul-q-nox 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.
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Sul-Q-Nox®
31.92% (Sulfaquinoxaline as sodium and potassium salts)
ANTIMICROBIAL
Manufactured for:
Huvepharma, Inc.
525 Westpark Drive, Suite 230
Peachtree City, GA 30269
HUVEPHARMA®
HUVEPHARMA and Sul-Q-Nox are registered
trademarks of Huvepharma EOOD
Approved by FDA under NADA # 006-891
P08-4001SL
Rev. 01-2022
Precautions
Caution: Federal (USA) law restricts this drug to use by or on the
order of a licensed veterinarian.
For Use in Animal Drinking Water Only
Sulfonamide
KEEP OUT OF REACH OF CHILDREN
KEEP TIGHTLY SEALED WHEN NOT IN USE
Restricted Drug (California) - Use only as directed. Not for human use.
Net Contents: 1 Gallon (128 fl. oz.)
General Precautions
CAUTION:
• May cause toxic reactions unless drug is evenly mixed in water at dosages indicated and used according
to directions.
• Levels of sulfaquinoxaline higher than 0.025% in feed or 0.012% in water for more than 24 to 36 hours
may result in reduced growth rate in chickens as a result of reduced feed or water intake.
• 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 necessary dosage of
approximately 10 to 45 mg/lb/day in chickens and 3.5 to 55 mg/lb/day in turkeys and 6 mg/lb/day in
cattle and calves, depending on class of animal, ambient temperature, age, and other factors.
• Prolonged administration of sulfaquinoxaline at higher doses may result in depressed feed or water
intake, deposition of sulfaquinoxaline crystals in kidney and interference with normal blood clotting.
• Do not mix or administer in galvanized containers.
• The follwing word is required on this product to comply with Agricultural Code of California:
HAZARDOUS
• CAUSES SKIN AND EYE BURNS. Avoid contact with eyes, skin, or clothing. In case of contact, flush
immediately with water for at least 15 minutes; for eye get medical attention.
Warnings
WARNING:
• Withdraw use of product 10 days before slaughter.
• A withdrawal period has not been established for this product in pre-ruminating
calves. Do not use in calves to be processed for veal.
• Do not medicate chickens or turkeys producing eggs for human
consumption.
• Not for use in lactating dairy cattle.
• DISPOSE OF ANY WASTE OR UNUSED PORTION PROPERLY.
• KEEP ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.
• Store between 20°- 25°C (68°- 77°F); excursions permitted between
15°- 40°C (59°- 104°F).
Indications & Usage
FOR AUTOMATIC DRINKING WATER PROPORTIONERS
FOR CONTROL OR TREATMENT OF THE FOLLOWING DISEASES WHEN CAUSED BY ONE
OR MORE PATHOGENIC ORGANISMS SUSCEPTIBLE TO SULFAQUINOXALINE
PREPARE MEDICATED DRINKING WATER FRESH DAILY
| INDICATIONS | DOSAGE PER 128 GALLONS OF WATER | TREATMENT |
| COCCIDIOSIS — CHICKENS: Control of coccidiosis caused by Eimeria tenella, E. necatrix, E. maxima, E. brunetti, E. acervulina, susceptible to sulfaquinoxaline. | 20½ fl. oz. (0.04%) | Give for 2-3 days, skip 3 days. Then |
| 13 fl. oz. (0.025%) | Give for 2 days more. If bloody droppings appear, repeat treatment at this level for 2 more days. CAUTION: Do not change litter unless absolutely necessary. Do not give flushing mashes. | |
| COCCIDIOSIS — TURKEYS: Control of coccidiosis caused by Eimeria meleagrimitis, E. adenoeides, susceptible to sulfaquinoxaline. | 13 fl. oz. (0.025%) | Give for 2 days - skip 3 days - give for 2 days - skip 3 days and give 2 more days. Repeat if necessary. CAUTION: Do not change litter unless absolutely necessary. Do not give flushing mashes. |
| ACUTE FOWL CHOLERA — CHICKENS AND TURKEYS: Control of acute fowl cholera caused by Pasteurella multocida susceptible to sulfaquinoxaline. FOWL TYPHOID — CHICKENS AND TURKEYS: Control of fowl typhoid caused by Salmonella gallinarum, susceptible to sulfaquinoxaline. | 20½ fl. oz. (0.04%) | Use for 2-3 days. Move birds to clean ground. If disease recurs, repeat treatment. Poultry that have survived fowl typhoid outbreaks should not be kept for laying house replacements or breeders unless tests show they are not carriers. |
| COCCIDIOSIS — CATTLE AND CALVES: For the control and treatment of coccidiosis caused by Eimeria bovis, E. zuernii, susceptible to sulfaquinoxaline. | 7¾ fl. oz. (0.015%) 6 mg/lb of body wt. | Give for 3-5 days. As a generalization, cattle and calves individually. |
| 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. | ||
* The information on this page is for an ANIMAL PRODUCT, please review the complete disclaimer below.