Malta - English - Medicines Authority

m & a pharmachem limited allenby laboratories, wigan road westhoughton, bolton, bl 5 2al, united kingdom - paracetamol - tablet - paracetamol 500 mg - analgesics

United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

waymade healthcare plc - paracetamol - oral capsule - 500mg

New Zealand - English - Medsafe (Medicines Safety Authority)

psm healthcare ltd trading as api consumer brands - domperidone maleate 12.72mg equivalent to domperidone 10 mg - tablet - 10 mg - active: domperidone maleate 12.72mg equivalent to domperidone 10 mg excipient: colloidal silicon dioxide lactose monohydrate magnesium stearate maize starch microcrystalline cellulose povidone purified water sodium laurilsulfate - treatment of acute symptoms of nausea and vomiting.

Australia - English - Department of Health (Therapeutic Goods Administration)

arrotex pharmaceuticals pty ltd - domperidone maleate, quantity: 12.72 mg (equivalent: domperidone, qty 10 mg) - tablet, uncoated - excipient ingredients: magnesium stearate; microcrystalline cellulose; colloidal anhydrous silica; povidone; sodium lauryl sulfate; lactose monohydrate; maize starch - apo-domperidone is indicated for the short-term treatment in adults of:,? symptoms associated with idiopathic or diabetic gastroparesis (once control of diabetes has been established by diet and/or insulin, an attempt should be made to discontinue apo-domperidone).,? intractable nausea and vomiting from any cause.

New Zealand - English - Medsafe (Medicines Safety Authority)

viatris limited - domperidone maleate 12.72mg equivalent to domperidone 10 mg - tablet - 10 mg - active: domperidone maleate 12.72mg equivalent to domperidone 10 mg excipient: colloidal silicon dioxide lactose monohydrate magnesium stearate maize starch microcrystalline cellulose povidone purified water sodium laurilsulfate - treatment of acute symptoms of nausea and vomiting.

Australia - English - Department of Health (Therapeutic Goods Administration)

arrotex pharmaceuticals pty ltd - tramadol hydrochloride, quantity: 37.5 mg; paracetamol, quantity: 325 mg - tablet, film coated - excipient ingredients: microcrystalline cellulose; stearic acid; hyprolose; croscarmellose sodium; titanium dioxide; iron oxide yellow; macrogol 8000; hypromellose; povidone; pregelatinised maize starch - tramadol/paracetamol is indicated for the short-term management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain.

Australia - English - Department of Health (Therapeutic Goods Administration)

arrotex pharmaceuticals pty ltd - paracetamol, quantity: 500 mg; codeine phosphate hemihydrate, quantity: 30 mg - tablet - excipient ingredients: magnesium stearate; stearic acid; povidone; pregelatinised maize starch - short-term management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain.

United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

alliance healthcare (distribution) ltd - paracetamol - oral capsule - 500mg

United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

kent pharma (uk) ltd - paracetamol - oral capsule - 500mg

United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

focus pharmaceuticals ltd - paracetamol - oral capsule - 500mg