Finasterid STADA Filmuhúðuð tafla 1 mg আইসলণ্ড - আইসল্যান্ডীয় - LYFJASTOFNUN (Icelandic Medicines Agency)

finasterid stada filmuhúðuð tafla 1 mg

stada arzneimittel ag - finasteridum inn - filmuhúðuð tafla - 1 mg

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

intrinsa

warner chilcott uk ltd. - testósterón - kynferðisleg truflun, sálfræðileg - hormón kynlíf og stillum kynfæri - intrinsa er ætlað fyrir meðferð hypoactive kynhvöt röskun (hsdd) í tvíhliða oophorectomised og hysterectomised (skurðaðgerð völdum tíðahvörf) konur fá aðra estrógen meðferð.

Alimemazin Evolan Hart hylki 20 mg আইসলণ্ড - আইসল্যান্ডীয় - LYFJASTOFNUN (Icelandic Medicines Agency)

alimemazin evolan hart hylki 20 mg

evolan pharma ab - alimemazinum tartrat - hart hylki - 20 mg

Risperdal Filmuhúðuð tafla 1 mg আইসলণ্ড - আইসল্যান্ডীয় - LYFJASTOFNUN (Icelandic Medicines Agency)

risperdal filmuhúðuð tafla 1 mg

janssen-cilag ab - risperidonum inn - filmuhúðuð tafla - 1 mg

Metformin Sandoz Filmuhúðuð tafla 500 mg আইসলণ্ড - আইসল্যান্ডীয় - LYFJASTOFNUN (Icelandic Medicines Agency)

metformin sandoz filmuhúðuð tafla 500 mg

sandoz a/s* - metforminum hýdróklóríð - filmuhúðuð tafla - 500 mg

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

mirvaso

galderma international - brimonidintartrat - húðsjúkdómar - aðrar húðsjúkdómar - mirvaso er ætlað til meðferðar við geðrofsroði rósroða hjá fullorðnum sjúklingum.

Travoprost/Timolol STADA Augndropar, lausn 40 míkróg/ml + 5 mg/ml আইসলণ্ড - আইসল্যান্ডীয় - LYFJASTOFNUN (Icelandic Medicines Agency)

travoprost/timolol stada augndropar, lausn 40 míkróg/ml + 5 mg/ml

stada arzneimittel ag - travoprostinum inn; timololum maleat - augndropar, lausn - 40 míkróg/ml + 5 mg/ml

Fixopost (Monoprostduo) Augndropar, lausn í stakskammtaíláti 50 míkróg/ml + 5 mg/ml আইসলণ্ড - আইসল্যান্ডীয় - LYFJASTOFNUN (Icelandic Medicines Agency)

fixopost (monoprostduo) augndropar, lausn í stakskammtaíláti 50 míkróg/ml + 5 mg/ml

laboratoires thea* - latanoprostum inn; timololum maleat - augndropar, lausn í stakskammtaíláti - 50 míkróg/ml + 5 mg/ml

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

coxevac

ceva santé animale - óvirkt coxiella burnetii bóluefni, stofn nine mile - immunologicals for bovidae, inactivated bacterial vaccines (including mycoplasma, toxoid and chlamydia) - goats; cattle - cattle: , for the active immunisation of cattle to lower the risk for non-infected animals vaccinated when non-pregnant to become shedder (5 times lower probability in comparison with animals receiving a placebo), and to reduce shedding of coxiella burnetii in these animals via milk and vaginal mucus. , onset of immunity: not established. , duration of immunity: 280 days after completion of the primary vaccination course. , goats: , for the active immunisation of goats to reduce abortion caused by coxiella burnetii and to reduce shedding of the organism via milk, vaginal mucus, faeces and placenta. , onset of immunity: not established. , duration of immunity: one year after completion of the primary vaccination course.

Kentera (previously Oxybutynin Nicobrand) ইউরোপীয় ইউনিয়ন - আইসল্যান্ডীয় - EMA (European Medicines Agency)

kentera (previously oxybutynin nicobrand)

teva b.v.  - oxybutynin - Þvagleki, þrá - Þvaglát - einkenni meðhöndlunar á þvagleka og / eða aukinni þvagfærasýkingu og bráðatilvikum sem geta komið fram hjá fullorðnum sjúklingum með óstöðuga þvagblöðru.