Emselex Европейски съюз - български - EMA (European Medicines Agency)

emselex

pharmaand gmbh - дарифенацин хидробромид - urinary incontinence, urge; urinary bladder, overactive - urologicals, лекарства за уриниране и инконтиненция - Симптоматично лечение на импулсна инконтиненция и / или повишена честота и спешност в урината, които могат да се появят при възрастни пациенти с синдром на свръхактивен пикочен мехур.

Tecfidera Европейски съюз - български - EMA (European Medicines Agency)

tecfidera

biogen netherlands b.v. - диметил фумарат - Множествена склероза - Имуносупресори - tecfidera is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

Maltofer 10 mg/ml syrup България - български - Изпълнителна агенция по лекарствата

maltofer 10 mg/ml syrup

vifor france sa - Желязо азотен полимальтозный комплекс - 10 mg/ml syrup

Maxitrol 3 500 IU/6 000 IU/1 mg/g eye ointment България - български - Изпълнителна агенция по лекарствата

maxitrol 3 500 iu/6 000 iu/1 mg/g eye ointment

Алкон България ЕООД - Дексаметазон, Неомицин, Полимиксин - 3 500 iu/6 000 iu/1 mg/g eye ointment

Maxitrol 3500 IU/6000 IU/1 mg/ml, eye drops, suspension България - български - Изпълнителна агенция по лекарствата

maxitrol 3500 iu/6000 iu/1 mg/ml, eye drops, suspension

Алкон България ЕООД - Дексаметазон, Неомицин, Полимиксин - 3500 iu/6000 iu/1 mg/ml, eye drops, suspension

Kriptazen Европейски съюз - български - EMA (European Medicines Agency)

kriptazen

virbac s.a. - халофугинонът - антипротозойни - Телета, новородено - in new born calves:- prevention of diarrhoea due to diagnosed cryptosporidium parvum, in farms with history of cryptosporidiosis,administration should start in the first 24 to 48 hours of age- reduction of diarrhoea due to diagnosed cryptosporidium parvum. Прилагането трябва да започне в рамките на 24 часа след началото на диарията. И в двата случая е доказано намаляването на екскрецията на ооцистите.

CEVAC SALMOVAC България - български - БАБХ (Българска агенция по безопасност на храните)

cevac salmovac

Сева Анимал Хелт България ЕООД - enteritidis салмонелл мутант, прецедете 441/014 - лиофилизат за пероралана суспензия - 1 до 8 х 10 на 8 степен cfu - пилета

PROGRESSIS България - български - БАБХ (Българска агенция по безопасност на храните)

progressis

Сева Анимал Хелт България ЕООД - Вирус репродуктивно & респираторно синдром (РРСС), инактивированная, щам p120 - инжекционна емулсия - ≥ 2.5 log10 if - прасета

STENOROL CRYPTO 0.5 mg/ml oral solution for calves 0.5 mg/ml България - български - БАБХ (Българска агенция по безопасност на храните)

stenorol crypto 0.5 mg/ml oral solution for calves 0.5 mg/ml

huvepharma nv - halofuginone - перорален разтвор - 0.5 mg/ml - говеда, телета

Comirnaty Европейски съюз - български - EMA (European Medicines Agency)

comirnaty

biontech manufacturing gmbh - single-stranded, 5’-capped messenger rna produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - Ваксини - comirnaty 30 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty original/omicron ba. 1 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older who have previously received at least a primary vaccination course against covid-19. comirnaty original/omicron ba. 4-5 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty original/omicron ba. 4-5 (1. 5/1. 5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty omicron xbb. 5 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty omicron xbb. 5 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 10 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years. Използването на тази ваксина трябва да бъде приложена в съответствие с официалните препоръки.