SLOW K 600 Milligram Tablet Prolonged Release Irlanda - inglês - HPRA (Health Products Regulatory Authority)

slow k 600 milligram tablet prolonged release

novartis pharmaceuticals uk ltd - potassium chloride - tablet prolonged release - 600 milligram

Prepandemic influenza vaccine (H5N1) (surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics União Europeia - inglês - EMA (European Medicines Agency)

prepandemic influenza vaccine (h5n1) (surface antigen, inactivated, adjuvanted) novartis vaccines and diagnostics

novartis vaccines and diagnostics s.r.l. - influenza virus surface antigens (haemagglutinin and neuraminidase) of strain a/viet nam/1194/2004 (h5n1) - influenza, human - vaccines - active immunisation against h5n1 subtype of influenza a virus.; this indication is based on immunogenicity data from healthy subjects from the age of 18 years onwards following administration of two doses of the vaccine containing a/vietnam/1194/2004 (h5n1)-like strain.; prepandemic influenza vaccine (h5n1) novartis vaccines and diagnostic should be used in accordance with official recommendations.

AMLODIPINE/VALSARTAN NOVARTIS 5/80 amlodipine 5 mg/valsartan 80 mg film-coated tablet blister pack Austrália - inglês - Department of Health (Therapeutic Goods Administration)

amlodipine/valsartan novartis 5/80 amlodipine 5 mg/valsartan 80 mg film-coated tablet blister pack

novartis pharmaceuticals australia pty ltd - amlodipine besilate, quantity: 6.94 mg (equivalent: amlodipine, qty 5 mg); valsartan, quantity: 80 mg - tablet, film coated - excipient ingredients: microcrystalline cellulose; magnesium stearate; crospovidone; colloidal anhydrous silica; titanium dioxide; hypromellose; purified talc; macrogol 4000; iron oxide yellow - amlodipine/valsartan novartis is indicated for the treatment of hypertension. treatment should not be initiated with this fixed dose combination.

Simulect 20mg powder and solvent for solution for injection vials Reino Unido - inglês - MHRA (Medicines & Healthcare Products Regulatory Agency)

simulect 20mg powder and solvent for solution for injection vials

novartis pharmaceuticals uk ltd - basiliximab - powder and solvent for solution for injection - 20mg

Simulect 10mg powder and solvent for solution for injection vials Reino Unido - inglês - MHRA (Medicines & Healthcare Products Regulatory Agency)

simulect 10mg powder and solvent for solution for injection vials

novartis pharmaceuticals uk ltd - basiliximab - powder and solvent for solution for injection - 10mg

Zometa 4mg5ml solution for infusion vials Reino Unido - inglês - MHRA (Medicines & Healthcare Products Regulatory Agency)

zometa 4mg5ml solution for infusion vials

novartis pharmaceuticals uk ltd - zoledronic acid monohydrate - solution for infusion - 800microgram/1ml