Страна: Канада
Язык: французский
Источник: Health Canada
Florfénicol
INTERVET CANADA CORP
300MG
Solution
Florfénicol 300MG
Intramusculaire
50/100/250/500ML
Prescription
Bétails; Bétails; Porcs
Numéro de groupe d'ingrédients actifs (GIA) :0128566001
APPROUVÉ
1999-03-19
Package Insert – EN 100 mL format only Version 27JAN2023 VETERINARY USE ONLY PR NUFLOR ® FLORFENICOL 300 MG/ML DIN 02216558 Sterile Injectable Antibiotic Solution For Intramuscular and Subcutaneous use in Beef and Non-lactating Dairy Cattle only, and for Intramuscular use in Swine. DESCRIPTION: NUFLOR is a light yellow to straw coloured, slightly viscous solution. Each milliliter contains; Active ingredient: 300 mg florfenicol; Inactive ingredients: 250 mg _N_-methyl-2-pyrrolidone (NMP), polyethylene glycol 300 q.s. 1.0 mL and 150 mg propylene glycol as a preservative. INDICATIONS: CATTLE: NUFLOR Injectable Solution is indicated for the treatment of bovine respiratory disease complex, also called shipping fever, associated with _Mannheimia haemolytica, Pasteurella multocida_ and _Histophilus somni _(_Haemophilus _ _somnus_). NUFLOR Injectable Solution is also indicated for the reduction of morbidity associated with bovine respiratory disease (BRD) in feedlot calves, caused by _Mannheimia haemolytica, Pasteurella multocida _and _Histophilus somni _(_Haemophilus _ _somnus_), during the first 28 days in the feedlot, when administered at the time of arrival. NUFLOR Injectable Solution is also indicated for the treatment of bovine interdigital phlegmon (foot rot, interdigital necrobacillosis, infectious pododermatitis) associated with _Fusobacterium necrophorum_ and _Bacteroides melaninogenicus_ and for the treatment of infectious bovine keratoconjunctivitis (IBK, Pinkeye) caused by _Moraxella _ _bovis_. SWINE: NUFLOR Injectable Solution is indicated for the treatment of swine respiratory diseases associated with _Actinobacillus pleuropneumoniae_ and _Pasteurella _ _multocida. _ DOSAGE AND ADMINISTRATION: CATTLE: NUFLOR Injectable Solution should be administered to cattle either by a single subcutaneous injection at a dose rate of 40 mg/kg body weight (6 mL/45 kg); or by intramuscular injection at a dose of 20 mg/kg body weight (3 mL/45 kg), a total of two doses with a 48 hour interval should be given. For feedlot Прочитать полный документ