ATAZANAVIR ACCORD 200 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

atazanavir accord 200 mg

pharmadox healthcare ltd. - malta - atazanavirum - caps. - 200mg - antivirale cu actiune directa inhibitori de proteaza

ATAZANAVIR ACCORD 300 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

atazanavir accord 300 mg

pharmadox healthcare ltd. - malta - atazanavirum - caps. - 300mg - antivirale cu actiune directa inhibitori de proteaza

Libtayo Uniunea Europeană - română - EMA (European Medicines Agency)

libtayo

regeneron ireland designated activity company (dac) - cemiplimab - carcinom, celule scuamoase - agenți antineoplazici - cutaneous squamous cell carcinomalibtayo as monotherapy is indicated for the treatment of adult patients with metastatic or locally advanced cutaneous squamous cell carcinoma (mcscc or lacscc) who are not candidates for curative surgery or curative radiation. basal cell carcinomalibtayo as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic basal cell carcinoma (labcc or mbcc) who have progressed on or are intolerant to a hedgehog pathway inhibitor (hhi). non-small cell lung cancerlibtayo as monotherapy is indicated for the first-line treatment of adult patients with non-small cell lung cancer (nsclc) expressing pd-l1 (in ≥ 50% tumour cells), with no egfr, alk or ros1 aberrations, who have:locally advanced nsclc who are not candidates for definitive chemoradiation, ormetastatic nsclc. libtayo in combination with platinum‐based chemotherapy is indicated for the first‐line treatment of adult patients with nsclc expressing pd-l1 (in ≥ 1% of tumour cells), with no egfr, alk or ros1 aberrations, who have:locally advanced nsclc who are not candidates for definitive chemoradiation, ormetastatic nsclc. cervical cancerlibtayo as monotherapy is indicated for the treatment of adult patients with recurrent or metastatic cervical cancer and disease progression on or after platinum-based chemotherapy.

LECIGON 20 mg/5 mg/20 mg/ml România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

lecigon 20 mg/5 mg/20 mg/ml

bioglan ab - suedia - combinatii (levodopum+carbidopum+entacaponum) - gel intestinal - 20mg/5mg/20mg/ml - agenti dopaminergici dopa si derivati

ATAZANAVIR ALVOGEN 150 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

atazanavir alvogen 150 mg

remedica ltd - cipru - atazanavirum - caps. - 150mg - antivirale cu actiune directa inhibitori de proteaza

ATAZANAVIR ALVOGEN 200 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

atazanavir alvogen 200 mg

remedica ltd - cipru - atazanavirum - caps. - 200mg - antivirale cu actiune directa inhibitori de proteaza

ATAZANAVIR ALVOGEN 300 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

atazanavir alvogen 300 mg

remedica ltd - cipru - atazanavirum - caps. - 300mg - antivirale cu actiune directa inhibitori de proteaza

Pemetrexed disodic 100 mg pulbere pentru concentrat pentru soluţie perfuzabilă Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

pemetrexed disodic 100 mg pulbere pentru concentrat pentru soluţie perfuzabilă

naprod life sciences private limited - pemetrexedum - pulbere pentru concentrat pentru soluţie perfuzabilă - 100 mg

Pemetrexed disodic 500 mg pulbere pentru concentrat pentru soluţie perfuzabilă Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

pemetrexed disodic 500 mg pulbere pentru concentrat pentru soluţie perfuzabilă

naprod life sciences private limited - pemetrexedum - pulbere pentru concentrat pentru soluţie perfuzabilă - 500 mg