Attentin Tafla 10 mg আইসলণ্ড - আইসল্যান্ডীয় - LYFJASTOFNUN (Icelandic Medicines Agency)

attentin tafla 10 mg

medice arzneimittel pütter gmbh & co. kg* - dexamfetaminum súlfat - tafla - 10 mg

Attentin Tafla 20 mg আইসলণ্ড - আইসল্যান্ডীয় - LYFJASTOFNUN (Icelandic Medicines Agency)

attentin tafla 20 mg

medice arzneimittel pütter gmbh & co. kg* - dexamfetaminum súlfat - tafla - 20 mg

Attentin Tafla 5 mg আইসলণ্ড - আইসল্যান্ডীয় - LYFJASTOFNUN (Icelandic Medicines Agency)

attentin tafla 5 mg

medice arzneimittel pütter gmbh & co. kg* - dexamfetaminum súlfat - tafla - 5 mg

Orfadin ইউরোপীয় ইউনিয়ন - আইসল্যান্ডীয় - EMA (European Medicines Agency)

orfadin

swedish orphan biovitrum international ab - nitisinón - tyrosinemias - Önnur meltingarvegi og efnaskipti vörur, - hereditary tyrosinemia type 1 (ht 1)orfadin is indicated for the treatment of adult and paediatric (in any age range) patients with confirmed diagnosis of hereditary tyrosinemia type 1 (ht 1) in combination with dietary restriction of tyrosine and phenylalanine. alkaptonuria (aku)orfadin is indicated for the treatment of adult patients with alkaptonuria (aku).

Betadine Baðlyf 75 mg/g আইসলণ্ড - আইসল্যান্ডীয় - LYFJASTOFNUN (Icelandic Medicines Agency)

betadine baðlyf 75 mg/g

mundipharma a/s - povidonum iodinatum inn - baðlyf - 75 mg/g

Atazanavir Mylan ইউরোপীয় ইউনিয়ন - আইসল্যান্ডীয় - EMA (European Medicines Agency)

atazanavir mylan

mylan pharmaceuticals limited - atazanavir (as sulfate) - hiv sýkingar - veirueyðandi lyf til almennrar notkunar - atazanavír mylan, gefið samhliða lágskammta ritonaviri, er ætlað til meðferðar við hiv 1 sýktum fullorðnum og börnum 6 ára og eldri í samsettri meðferð með öðrum andretróveirulyfjum. byggt á boði veirufræðilega og klínískum gögn úr fullorðinn sjúklingar, ekkert gagn er væntanlegur í sjúklingum við stofnum þola margar próteasahemlar (stærri 4 pi stökkbreytingar). takmarkaðar upplýsingar liggja fyrir frá börnum 6 ára og yngri en 18 ára. val á atazanavír mylan í meðferð upplifað fullorðna og börn sjúklingar ætti að vera byggt á einstökum veiru mótstöðu próf og sjúklings meðferð sögu.

Tegretol Mixtúra, dreifa 20 mg/ml আইসলণ্ড - আইসল্যান্ডীয় - LYFJASTOFNUN (Icelandic Medicines Agency)

tegretol mixtúra, dreifa 20 mg/ml

novartis healthcare a/s - carbamazepinum inn - mixtúra, dreifa - 20 mg/ml

Tegretol Tafla 200 mg আইসলণ্ড - আইসল্যান্ডীয় - LYFJASTOFNUN (Icelandic Medicines Agency)

tegretol tafla 200 mg

novartis healthcare a/s - carbamazepinum inn - tafla - 200 mg

Tegretol Retard Forðatafla 200 mg আইসলণ্ড - আইসল্যান্ডীয় - LYFJASTOFNUN (Icelandic Medicines Agency)

tegretol retard forðatafla 200 mg

novartis healthcare a/s - carbamazepinum inn - forðatafla - 200 mg

Tegretol Retard Forðatafla 400 mg আইসলণ্ড - আইসল্যান্ডীয় - LYFJASTOFNUN (Icelandic Medicines Agency)

tegretol retard forðatafla 400 mg

novartis healthcare a/s - carbamazepinum inn - forðatafla - 400 mg