माल्टा - अंग्रेज़ी - Medicines Authority

viatris limited damastown industrial park, mulhuddart, dublin 15, dublin, ireland - film-coated tablet - eletriptan hydrobromide 40 mg - analgesics

न्यूज़ीलैंड - अंग्रेज़ी - Medsafe (Medicines Safety Authority)

viatris limited - bisacodyl 5mg - enteric coated tablet - 5 mg - active: bisacodyl 5mg excipient: carnauba wax hyprolose hypromellose methacrylic acid copolymer, eudragit s 100 iron oxide yellow isopropyl alcohol lactose monohydrate magnesium stearate   methacrylic acid copolymer microcrystalline cellulose purified talc purified water   starch sucrose titanium dioxide triethyl citrate - short term relief of constipation

न्यूज़ीलैंड - अंग्रेज़ी - Medsafe (Medicines Safety Authority)

viatris limited - lamivudine 150mg; zidovudine 300mg - film coated tablet - active: lamivudine 150mg zidovudine 300mg excipient: colloidal silicon dioxide magnesium stearate microcrystalline cellulose opadry white propylene glycol purified water sodium starch glycolate - indicated for the treatment of hiv infected adults and adolescents over the age of 12 years, with progressive immunodeficiency (cd4+ count = < 500 cells/mm³).

न्यूज़ीलैंड - अंग्रेज़ी - Medsafe (Medicines Safety Authority)

viatris limited - tenofovir disoproxil maleate 300mg equivalent to tenofovir disoproxil 245mg - film coated tablet - 300 mg - active: tenofovir disoproxil maleate 300mg equivalent to tenofovir disoproxil 245mg excipient: colloidal silicon dioxide hyprolose lactose monohydrate magnesium stearate microcrystalline cellulose opadry blue 32k505018 - tenofovir disoproxil mylan is indicated for the treatment of chronic hepatitis b in adults and paediatric patients 12 years of age and older.

न्यूज़ीलैंड - अंग्रेज़ी - Medsafe (Medicines Safety Authority)

viatris limited - lamivudine 150mg;  ;   - film coated tablet - 150 mg - active: lamivudine 150mg     excipient: magnesium stearate microcrystalline cellulose opadry white propylene glycol purified water sodium starch glycolate - lamuvidine in combination with other anti-retroviral agents is indicated for the treatment of hiv-infected adults and children.

न्यूज़ीलैंड - अंग्रेज़ी - Medsafe (Medicines Safety Authority)

viatris limited - nevirapine 200mg (based on 100% assay and nil water content);   - tablet - 200 mg - active: nevirapine 200mg (based on 100% assay and nil water content)   excipient: colloidal silicon dioxide lactose monohydrate magnesium stearate microcrystalline cellulose povidone purified water sodium starch glycolate - use in combination with other antiretroviral agents for the treatment of hiv-1 infection in adults. resistant virus emerges rapidly and uniformly when nevirapine is administered as monotherapy. therefore, it should always be administered in combination with at least two additional antiretroviral agents.

न्यूज़ीलैंड - अंग्रेज़ी - Medsafe (Medicines Safety Authority)

viatris limited - valganciclovir hydrochloride 496.3mg equivalent to valganciclovir 450 mg - film coated tablet - 450 mg - active: valganciclovir hydrochloride 496.3mg equivalent to valganciclovir 450 mg excipient: crospovidone microcrystalline cellulose opadry brown 15b565009 purified water stearic acid - for the treatment of cytomegalovirus (cmv) retinitis in acquired immunodeficiency syndrome (aids) patients. for the prevention of cmv disease in solid organ transplant patients at risk.

आयरलैंड - अंग्रेज़ी - HPRA (Health Products Regulatory Authority)

viatris limited - atorvastatin calcium trihydrate - film-coated tablet - hmg coa reductase inhibitors; atorvastatin

आयरलैंड - अंग्रेज़ी - HPRA (Health Products Regulatory Authority)

viatris limited - atorvastatin calcium trihydrate - film-coated tablet - hmg coa reductase inhibitors; atorvastatin

आयरलैंड - अंग्रेज़ी - HPRA (Health Products Regulatory Authority)

viatris limited - atorvastatin calcium trihydrate - film-coated tablet - hmg coa reductase inhibitors; atorvastatin