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Item No.
52926
Cefenil RTU (Ceftiofur Hydrochloride) 50 mg/mL Injectable for Cattle and Swine Rx
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Product Description
Cefenil RTU (Ceftiofur Hydrochloride) 50 mg/mL is indicated for treatment/control of the following:
In Swine bacterial respiratory disease (swine bacterial pneumonia) associated with Actinobacillus (Haemophilus) pleuropneumoniae, Pasteurella multocida, Salmonella choleraesuis and Streptococcus suis.
In Cattle it is indicated for treatment of the following bacterial diseases:
- Bovine respiratory disease (BRD, shipping fever, pneumonia) associated with Mannheimia haemolytica, Pasteurella multocida and Histophilus somni.
- Acute bovine interdigital necrobacillosis (foot rot, pododermatitis) associated with Fusobacterium necrophorum and Bacteroides melaninogenicus.
- Acute metritis (0 to 14 days post-partum) associated with bacterial organisms susceptible to ceftiofur.
Who is Cefenil RTU (Ceftiofur Hydrochloride) 50 mg/mL Injectable for Cattle and Swine for?
Cattle and Swine
Why use Cefenil RTU (Ceftiofur Hydrochloride) 50 mg/mL Injectable for Cattle and Swine?
Helps treat : Swine bacterial respiratory disease, Bovine respiratory disease, Acute bovine interdigital necrobacillosis (foot rot, pododermatitis) and Acute metritis (0 to 14 days post-partum) associated with bacterial organisms susceptible to ceftiofur.
How does Cefenil RTU (Ceftiofur Hydrochloride) 50 mg/mL Injectable for Cattle and Swine work?
CEFENIL RTU (ceftiofur hydrochloride sterile suspension) is a ready to use formulation that contains the hydrochloride salt of ceftiofur, which is a broad spectrum cephalosporin antibiotic.
Manufacturer:
Norbrook
Active Ingredients(s):
Ceftiofur Hydrochloride
How is Cefenil RTU (Ceftiofur Hydrochloride) 50 mg/mL Injectable for Cattle and Swine sold?
Sold in vials of 100 ml and 250 ml.
What are the side effects of Cefenil RTU (Ceftiofur Hydrochloride) 50 mg/mL Injectable for Cattle and Swine?
Contraindications: As with all drugs, the use of CEFENIL RTU is contraindicated in animals previously found to be hypersensitive to the drug.
What special precautions are there?
Warnings
NOT FOR HUMAN USE. KEEP OUT OF REACH OF CHILDREN.
Penicillins and cephalosporins can cause allergic reactions in sensitized individuals. Topical exposures to such antimicrobials, including ceftiofur, may elicit mild to severe allergic reactions in some individuals. Repeated or prolonged exposure may lead to sensitization. Avoid direct contact of the product with the skin, eyes, mouth, and clothing. Persons with a known hypersensitivity to penicillin or cephalosporins should avoid exposure to this product. In case of accidental eye exposure, flush with water for 15 minutes. In case of accidental skin exposure, wash with soap and water. Remove contaminated clothing. If allergic reaction occurs (e.g., skin rash, hives, difficult breathing), seek medical attention. The effects of ceftiofur on cattle and swine reproductive performance, pregnancy, and lactation have not been determined.
What to do if overdose?
Contact your nearest emergency animal hospital.
How can I store Cefenil RTU (Ceftiofur Hydrochloride) 50 mg/mL Injectable for Cattle and Swine?
Do not store above 30°C (86°F). Shake well before using. Protect from freezing. Contents should be used within 42 days after the first dose is removed.
Overview
Use as directed by your Veterinarian.
Cefenil RTU Dosage And Administration
Shake for 90 seconds to ensure complete resuspension before using.
Swine: Administer intramuscularly at a dosage of 1.36 to 2.27 mg ceftiofur equivalents/lb (3.0 to 5.0 mg/kg) BW (1 mL of sterile suspension per 22 to 37 lb BW). Treatment should be repeated at 24 h intervals for a total of three consecutive days.
Cattle: - For bovine respiratory disease and acute bovine interdigital necrobacillosis: administer by intramuscular or subcutaneous administration at the dosage of 0.5 to 1.0 mg ceftiofur equivalents/lb (1.1 to 2.2 mg/kg) BW (1 to 2 mL sterile suspension per 100 lb BW). Administer daily at 24 h intervals for a total of three consecutive days. Additional treatments may be administered on Days 4 and 5 for animals which do not show a satisfactory response (not recovered) after the initial three treatments. In addition, for BRD only, administer intramuscularly or subcutaneously 1.0 mg ceftiofur equivalents/lb (2.2 mg/kg) BW every other day on Days 1 and 3 (48 h interval). Do not inject more than 15 mL per injection site. Selection of dosage level (0.5 to 1.0 mg/lb) and regimen/duration (daily or every other day for BRD only) should be based on an assessment of the severity of disease, pathogen susceptibility and clinical response.
- For acute post-partum metritis: administer by intramuscular or subcutaneous administration at the dosage of 1.0 mg ceftiofur equivalents/lb (2.2 mg/kg) BW (2 mL sterile suspension per 100 lb BW). Administer at 24 h intervals for five consecutive days. Do not inject more than 15 mL per injection site.
Main Ingredients
(ceftiofur hydrochloride sterile suspension)
Equivalent to 50 mg per mL ceftiofur