ENROFLOXACIN FLAVORED- enrofloxacin tablet, chewable United States - English - NLM (National Library of Medicine)

enrofloxacin flavored- enrofloxacin tablet, chewable

putney, inc. - enrofloxacin (unii: 3dx3xek1bn) (enrofloxacin - unii:3dx3xek1bn) - enrofloxacin 22.7 mg - enrofloxacin flavored tablets are indicated for the management of diseases associated with bacteria susceptible to enrofloxacin. enrofloxacin flavored tablets are indicated for use in dogs and cats. enrofloxacin is contraindicated in dogs and cats known to be hypersensitive to quinolones. dogs: based on the studies discussed under the section on animal safety summary, the use of enrofloxacin is contraindicated in small and medium breeds of dogs during the rapid growth phase (between 2 and 8 months of age). the safe use of enrofloxacin has not been established in large and giant breeds during the rapid growth phase. large breeds may be in this phase for up to one year of age and the giant breeds for up to 18 months. in clinical field trials utilizing a daily oral dose of 5.0 mg/kg, there were no reports of lameness or joint problems in any breed. however, controlled studies with histological examination of the articular cartilage have not been conducted in the large or giant breeds.

ENROFLOXACIN injection solution United States - English - NLM (National Library of Medicine)

enrofloxacin injection solution

putney, inc. - enrofloxacin (unii: 3dx3xek1bn) (enrofloxacin - unii:3dx3xek1bn) - enrofloxacin 22.7 mg in 1 ml

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

enrofloxacin solution

butler animal health supply, llc dba covetrus north america - enrofloxacin (unii: 3dx3xek1bn) (enrofloxacin - unii:3dx3xek1bn) - enrofloxacin injectable solution is indicated for the management of diseases in dogs associated with bacteria susceptible to enrofloxacin. enrofloxacin is contraindicated in dogs known to be hypersensitive to quinolones. based on the studies discussed under the section on animal safety summary, the use of enrofloxacin is contraindicated in small and medium breeds of dogs during the rapid growth phase (between 2 and 8 months of age). the safe use of enrofloxacin has not been established in large and giant breeds during the rapid growth phase. large breeds may be in this phase for up to one year of age and the giant breeds for up to 18 months. in clinical field trials utilizing a daily oral dose of 5.0 mg/kg, there were no reports of lameness or joint problems in any breed. however, controlled studies with histological examination of the articular cartilage have not been conducted in the large or giant breeds.

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

enrofloxacin powder

yicheng chemical corp. - enrofloxacin (unii: 3dx3xek1bn) (enrofloxacin - unii:3dx3xek1bn) - enrofloxacin 1 kg in 1 kg

ENROFLOXACIN BASE powder United States - English - NLM (National Library of Medicine)

enrofloxacin base powder

darmerica - enrofloxacin (unii: 3dx3xek1bn) (enrofloxacin - unii:3dx3xek1bn) - enrofloxacin 1 kg in 1 kg

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

enrofloxacin powder

attix pharmaceuticals - enrofloxacin (unii: 3dx3xek1bn) (enrofloxacin - unii:3dx3xek1bn) - enrofloxacin 5 kg in 5 kg

ENROFLOXACIN HCL powder United States - English - NLM (National Library of Medicine)

enrofloxacin hcl powder

attix pharmaceuticals - enrofloxacin (unii: 3dx3xek1bn) (enrofloxacin - unii:3dx3xek1bn) - enrofloxacin 5 kg in 5 kg

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

enrofloxacin powder

professional compounding centers of america dba pcca - enrofloxacin (unii: 3dx3xek1bn) (enrofloxacin - unii:3dx3xek1bn) - enrofloxacin usp for veterinary use only *protect from light* for prescription compounding/rx only part: 30-4815 gm cas: 93106-60-6 danger: harmful substance. irritating substance. may cause eye, skin or respiratory irritation. possible hypersensitization. avoid raising and breathing dust use adequate ventilation. avoid alkalies. emits toxic fumes under fire conditions. wash thoroughly after handling. store in tightly closed container. preserve in well-closed,light resistant container. store at room temperature.

BAYTRIL OTIC- enrofloxacin/silver sulfadiazine emulsion United States - English - NLM (National Library of Medicine)

baytril otic- enrofloxacin/silver sulfadiazine emulsion

bayer healthcare llc animal health division - enrofloxacin (unii: 3dx3xek1bn) (enrofloxacin - unii:3dx3xek1bn), silver sulfadiazine (unii: w46jy43ejr) (sulfadiazine - unii:0n7609k889) - enrofloxacin 5 mg in 1 ml - baytril® otic is indicated as a treatment for canine otitis externa complicated by bacterial and fungal organisms susceptible to enrofloxacin and/or silver sulfadiazine (see microbiology section). baytril® otic is contraindicated in dogs with suspected or known hypersensitivity to quinolones and/or sulfonamides.

ENROFLOX- enrofloxacin injection, solution United States - English - NLM (National Library of Medicine)

enroflox- enrofloxacin injection, solution

norbrook laboratories limited - enrofloxacin (unii: 3dx3xek1bn) (enrofloxacin - unii:3dx3xek1bn) - enrofloxacin 22.7 mg in 1 ml - enroflox® (brand of enrofloxacin) injectable solution is indicated for the management of diseases in dogs associated with bacteria susceptible to enrofloxacin. enrofloxacin is contraindicated in dogs known to be hypersensitive to quinolones. based on the studies discussed under the section on animal safety summary, the use of enrofloxacin is contraindicated in small and medium breeds of dogs during the rapid growth phase (between 2 and 8 months of age). the safe use of enrofloxacin has not been established in large and giant breeds during the rapid growth phase. large breeds may be in this phase for up to one year of age and the giant breeds for up to 18 months. in clinical field trials utilizing a daily oral dose of 5.0 mg/kg, there were no reports of lameness or joint problems in any breed. however, controlled studies with histological examination of the articular cartilage have not been conducted in the large or giant breeds.