Ireland - Inggeris - HPRA (Health Products Regulatory Authority)

novartis ireland limited - diclofenac potassium - coated tablet - 50 milligram(s) - acetic acid derivatives and related substances; diclofenac

Malta - Inggeris - Medicines Authority

nm pharma limited 3/4, cantrija complex triq it-targa, il-maghtab naxxar nxr 6613 , malta - diclofenac potassium - tablet - diclofenac potassium 50 mg - antiinflammatory and antirheumatic products

New Zealand - Inggeris - Medsafe (Medicines Safety Authority)

novartis consumer health australasia pty ltd (nz) - diclofenac potassium 25mg;  ;   - tablet - 25 mg - active: diclofenac potassium 25mg     excipient: calcium phosphate colloidal silicon dioxide iron oxide red macrogol 8000 magnesium stearate maize starch microcrystalline cellulose opacode brown s-1-9210hv povidone   purified talc sodium starch glycolate sucrose titanium dioxide

Namibia - Inggeris - Namibia Medicines Regulatory Council

novartis south africa (pty) ltd - diclofenac potassium - powder for oral solution - one cataflam sachet powder for oral solution contains diclofenac potassium 50,0 mg

Singapura - Inggeris - HSA (Health Sciences Authority)

novartis (singapore) pte ltd - diclofenac resinate eqv diclofenac sodium - solution - 15 mg/ml

Ireland - Inggeris - HPRA (Health Products Regulatory Authority)

novartis pharmaceuticals uk ltd - diclofenac potassium - coated tablets - 25 milligram

Ireland - Inggeris - HPRA (Health Products Regulatory Authority)

novartis pharmaceuticals uk ltd - diclofenac potassium - powder for oral solution - 50 milligram

Ireland - Inggeris - HPRA (Health Products Regulatory Authority)

novartis pharmaceuticals uk ltd - diclofenac potassium - coated tablets - 25 milligram

Ireland - Inggeris - HPRA (Health Products Regulatory Authority)

novartis pharmaceuticals uk ltd - diclofenac potassium - coated tablets - 50 milligram - acetic acid derivatives and related substances