Veterinary Medicine Sulfamonomethoxine Sodium Injection for Animal
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| Varieties: | General Disease Prevention Medicine |
| Component: | Chemical Synthetic Drugs |
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Year of Establishment
1999-04-02
Number of Employees
1200
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Basic Info.
- Model NO.
- Sulfamonomethoxine Sodium Injection
- Type
- The First Class
- Pharmacodynamic Influential Factors
- Animal Species
- Storage Method
- Light Proof
- Veterinary Reg. No.
- 220042570
- Main Content
- Sulfamonomethoxine Sodium
- Usage
- Injection
- GMP
- 22018
- Expiry Date
- 2 Years
- Character
- a Clear, Colorless to Slightly Yellow Liquid
- Transport Package
- Box
- Specification
- 10ml/vial
- Trademark
- SINDER
- Origin
- Sichuan, China
- HS Code
- 2941909099
- Production Capacity
- 100000L/Year
Packaging & Delivery
- Package Size
- 45.00cm * 31.00cm * 23.00cm
- Package Gross Weight
- 9.300kg
Product Description
Sulfamonomethoxine Sodium Injection
Veterinary Use
(Veterinary Drug name)Sulfamonomethoxine Sodium Injection
(Main Component)Sulfamonomethoxine Sodium
(Description)A clear, colorless to slightly yellow liquid.
(Drug-Drug Interaction)
1. When the product is used with TMP (Antibacterial synerists) together, it has synergetic effect.
2. It will reduce the effect when the product is used with following drugs, like Procaine, Tetracaine and yeast.
3. It could worsen toxicity of kidney when the product is used with Diuretic, like
Thiazine or Furosemide.
(Indications for Use)Antimicrobials of Sulfonamides. The product is used for infections caused by sensitive bacteria,which is also used for pig's Toxoplasma infection.
(Administration and Dosage)
Intravenous injection, 0.5ml per 1kg weight of livestock for each dosage. 1-2 dosage/day, continuously use for 2 to 3 days.
(Adverse Effect)
1. Sulfanilamide or its metabolin will produce sediment in urine. It will be much easier to get crystal after high dose administration or low dose administration for long term, which will cause crystalluria, hematuresis or kidney tubules blockage.
2. Intravenous injection to horse may cause temporary paralysis.
3. PH value of this product is strong alkaline solutions, it has strong irritative to tissue.
(Precaution)
1. This product could produce crystal with acid, so it could not be diluted by 5% of Glucose liquid.
2. It will produce crystalluria when use for long term or high dose administration, the product shall be together used with Sodium Bicarbonate, and large quantity of water should be given to the livestock.
3. Stop using when anaphylaxis or other serious adverse effect happen, and give symptomatic treatment.
(Withdrawl)
28 days, 7 days from withdrawal period for milk.
| Specification | 5ml:0.5g |
| Package | 10ml/vial,10vials/box |
Approval No.: Veterinary drug 220042570
Executive Standard: <Chinese Veterinary Pharmacopoeia>, 2015 version, 1st section.
Producing License No.: (2015) Veterinary drug 22004.
Veterinary GMP Approval No.: (2015) Veterinary drug GMP No.22018.
Address: Zitong Economic zone, Mianyang, Sichuan Province, China.
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