Bretland - enska - MHRA (Medicines & Healthcare Products Regulatory Agency)

zentiva pharma uk ltd - citalopram hydrobromide - oral tablet - 20mg

Bretland - enska - MHRA (Medicines & Healthcare Products Regulatory Agency)

zentiva pharma uk ltd - citalopram hydrobromide - oral tablet - 40mg

Bretland - enska - MHRA (Medicines & Healthcare Products Regulatory Agency)

zentiva pharma uk ltd - lamotrigine - oral tablet - 200mg

Bretland - enska - MHRA (Medicines & Healthcare Products Regulatory Agency)

zentiva pharma uk ltd - sertraline hydrochloride - oral tablet - 50mg

Bretland - enska - MHRA (Medicines & Healthcare Products Regulatory Agency)

zentiva pharma uk ltd - sertraline hydrochloride - oral tablet - 100mg

Bretland - enska - MHRA (Medicines & Healthcare Products Regulatory Agency)

zentiva pharma uk ltd - glimepiride - oral tablet - 1mg

Bretland - enska - MHRA (Medicines & Healthcare Products Regulatory Agency)

zentiva pharma uk ltd - gabapentin - oral tablet - 600mg

Bretland - enska - MHRA (Medicines & Healthcare Products Regulatory Agency)

zentiva pharma uk ltd - gabapentin - oral tablet - 800mg

Bretland - enska - MHRA (Medicines & Healthcare Products Regulatory Agency)

zentiva pharma uk ltd - letrozole - oral tablet - 2.5mg

Evrópusambandið - enska - EMA (European Medicines Agency)

zentiva k.s. - efavirenz, emtricitabine, tenofovir disoproxil, phosphate - hiv infections - antivirals for systemic use, - efavirenz/emtricitabine/tenofovir disoproxil zentiva is a fixed-dose combination of efavirenz, emtricitabine and tenofovir disoproxil. it is indicated for the treatment of human immunodeficiency virus-1 (hiv-1) infection in adults aged 18 years and over with virologic suppression to hiv-1 rna levels of < 50 copies/ml on their current combination antiretroviral therapy for more than three months. patients must not have experienced virological failure on any prior antiretroviral therapy and must be known not to have harboured virus strains with mutations conferring significant resistance to any of the three components contained in efavirenz/emtricitabine/tenofovir disoproxil zentiva prior to initiation of their first antiretroviral treatment regimen., the demonstration of the benefit of the combination efavirenz/emtricitabine/tenofovir disoproxil is primarily based on 48-week data from a clinical study in which patients with stable virologic suppression on a combination antiretroviral therapy changed to efavir