Oxytetracycline and Flunixin Meglumine Injection For veterinary use only
Composition
Each ml contains Oxytetracycline 100mg and Flunixin meglumine 2mg.
Indications
For the control and treatment of infectious diseases of cattle caused by or associated with organisms sensitive to oxytetracycline, where concurrent analgesic, anti-inflammatory, anti-endotoxic or antipyretic therapy is desired. The product is especially indicated for the treatment of respiratory disease (particularly that associated with Mannheimia and Pasteurella infection) and acute mastitis (in conjunction with appropriate intramammary therapy).
Dosage and administration
For intramuscular injection.
Cattle: 1 ml/10 kg body weight daily for up to 5 days.
Adverse raction
Prolonged use of NSAIDs, including flunixin, may predispose or lead to gastrointestinal ulceration.
Reports of adverse reactions associated with oxytetracycline administration include injection site swelling, restlessness, ataxia, trembling, swelling of eyelids, ears, muzzle, anus and vulva (or scrotum and sheath in males), respiratory abnormalities (labored breathing), frothing at the mouth, collapse and possibly death. Some of these reactions may be attributed either to anaphylaxis (an allergic reaction) or to cardiovascular collapse of unknown cause.
Special warnings
Do not administer other NSAIDs concurrently or within 24 hours of each other.
Do not inject more than 20 ml intramuscularly at a single site.
Withdrawal period
Meat: 21 days.
Do not use in cattle producing milk for human consumption.
Storage
Seal and protect from light.
Keep out of reach of children.
Packing
50ml/100ml/bottle
Shelf life
3year
Veterinary Medicine GMP Certificate, Veterinary Medicine Production License
Quality Management System ISO9001, Environmental Management System ISO14001, Health Management System ISO45001
Model Unit of International Cooperation in Hebei Province
Top 30 Veterinary Medicine Enterprises in Hebei Province
Top 10 Veterinary Medicine Export Enterprises in Hebei Province
Are you a manufacturer? |
Yes, Shimu Group is a professional manufacturer established in 2001, located in Shijiazhuang high-tech industrial zone. Shimu Group is a comprehensive high-tech enterprise specialized in R&D, production, markering and technical service for veterinary drug and feed additive. |
Do you have GMP? |
Yes, the first GMP certification successfully got in 2005, and the latest GMP was updated in 2022. |
How does your factory control the quality? |
The company makes quality management as the focus of each work, and always implements the quality policy of "quality first, faithful and honest as the root". Quality Management Department consists of Quality Assurance Department (QA) and Quality Control Department-Central Laboratory (QC). The QC central laboratory is equipped with advanced inspection instruments and equipment that are compatible with the production scale. The existing quality inspectors all have years of experience in quality inspection of veterinary drug, and can independently judge and complete various inspection and monitoring work involved in the company's products, and have the ability to ensure that unqualified materials or intermediate products will not enter the next process. |
What certificates do you have? |
We have Manufacturing License and GMP. Also we have passed the certification of ISO9001, ISO 14001 and ISO45001. |
Can you provide registration? |
We have a professional registration team. We can provide registration documents for you. The documents include FSC, COPP, COA, Analysis Method, SMF, Stability Report, Instruction, and etc. |
Can we visit your company? |
Every year, many foreign customers come to visit our company. Welcome to visit our company.Shimu pharmaceutical co.,ltd which is veterinary medicine factory. |