United Kingdom - English - VMD (Veterinary Medicines Directorate)

norbrook laboratories limited - ceftiofur - powder and solvent for solution for injection - antimicrobial - cattle, pigs

United Kingdom - English - VMD (Veterinary Medicines Directorate)

norbrook laboratories limited - ceftiofur - powder and solvent for solution for injection - antimicrobial - cattle, horses, pigs

Ireland - English - HPRA (Health Products Regulatory Authority)

norbrook laboratories limited - ceftiofur - powder for solution for injection - 50 milligram(s)/millilitre - ceftiofur - cattle, pigs - antibacterial

Ireland - English - HPRA (Health Products Regulatory Authority)

norbrook laboratories (ireland) limited - ceftiofur - powder for solution for injection - 50 milligram(s)/millilitre - ceftiofur

United States - English - NLM (National Library of Medicine)

norbrook laboratories limited - ceftiofur hydrochloride (unii: 6822a07436) (ceftiofur - unii:83jl932i1c) - swine: cefenil rtu is indicated for treatment/control of swine bacterial respiratory disease (swine bacterial pneumonia) associated with actinobacillus (haemophilus) pleuropneumoniae , pasteurella multocida, salmonella choleraesuis and streptococcus suis . cattle: cefenil rtu is indicated for treatment of the following bacterial diseases: as with all drugs, the use of cefenil rtu is contraindicated in animals previously found to be hypersensitive to the drug.

United States - English - NLM (National Library of Medicine)

aspen veterinary resources - ceftiofur hydrochloride (unii: 6822a07436) (ceftiofur - unii:83jl932i1c) - swine: cefenil rtu is indicated for treatment/control of swine bacterial respiratory disease (swine bacterial pneumonia) associated with actinobacillus (haemophilus) pleuropneumoniae, pasteurella multocida, salmonella choleraesuis and streptococcus suis. cattle: cefenil rtu is indicated for treatment of the following bacterial diseases: 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 interdigitai necrobaciilosis: 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

Ireland - English - HPRA (Health Products Regulatory Authority)

norbrook laboratories limited - ceftiofur sodium - pdr for soln for injection - 50 mg/ml - ceftiofur - bovine, porcine - antibacterial

Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

norbrook laboratories (ireland) ltd. - ceftiofur sodium - eq. ceftiofur 50 mg/ml - powder and solvent for solution for injection - 50 mg/ml - ceftiofur sodium - ceftiofur - cattle; pig

Ireland - English - HPRA (Health Products Regulatory Authority)

norbrook laboratories limited - ceftiofur (as hydrochloride) - suspension for injection - 50 mg/ml - ceftiofur - bovine, porcine - antibacterial

United Kingdom - English - VMD (Veterinary Medicines Directorate)

norbrook laboratories limited - ceftiofur - suspension for injection - antimicrobial - cattle, pigs