New Zealand - English - Medsafe (Medicines Safety Authority)

viatris limited - donepezil hydrochloride 5mg equivalent to 4.56 mg donepezil base;   - film coated tablet - 5 mg - active: donepezil hydrochloride 5mg equivalent to 4.56 mg donepezil base   excipient: hyprolose lactose monohydrate magnesium stearate maize starch microcrystalline cellulose opadry white y-1-7000

New Zealand - English - Medsafe (Medicines Safety Authority)

pfizer new zealand limited - donepezil hydrochloride 5mg equivalent to 4.56 mg donepezil free base - film coated tablet - 5 mg - active: donepezil hydrochloride 5mg equivalent to 4.56 mg donepezil free base excipient: hyprolose lactose monohydrate magnesium stearate maize starch microcrystalline cellulose opadry white ys-1r-18134-a purified water  

Malta - English - Medicines Authority

wockhardt uk limited ash road north, wrexham, ll13 9uf, united kingdom - donepezil hydrochloride - film-coated tablet - donepezil hydrochloride 5 mg - psychoanaleptics

Malta - English - Medicines Authority

aurobindo pharma (malta) limited vault 14, level 2, valletta waterfront, floriana frn 1913, malta - donepezil hydrochloride - film-coated tablet - donepezil hydrochloride 5 mg - psychoanaleptics

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

generic health pty ltd - donepezil hydrochloride, quantity: 10 mg - tablet, film coated - excipient ingredients: hyprolose; iron oxide yellow; microcrystalline cellulose; titanium dioxide; macrogol 6000; hypromellose; maize starch; sodium stearylfumarate; lactose monohydrate; purified talc - donepezil is indicated for the treatment of mild, moderate and severe alzheimer's disease.

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

generic health pty ltd - donepezil hydrochloride, quantity: 5 mg - tablet, film coated - excipient ingredients: macrogol 6000; maize starch; lactose monohydrate; titanium dioxide; purified talc; microcrystalline cellulose; sodium stearylfumarate; hypromellose; hyprolose - donepezil is indicated for the treatment of mild, moderate and severe alzheimer's disease.

New Zealand - English - Medsafe (Medicines Safety Authority)

rex medical ltd - donepezil hydrochloride 5mg - film coated tablet - 5 mg - active: donepezil hydrochloride 5mg excipient: colloidal silicon dioxide croscarmellose sodium lactose monohydrate magnesium stearate microcrystalline cellulose opadry white 04f58804 purified water starch - donepezil tablets are indicated for the treatment of mild, moderate and severe alzheimer's disease.

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

teva pharma australia pty ltd - donepezil hydrochloride -

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

teva pharma australia pty ltd - donepezil hydrochloride -

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

alphapharm pty ltd - donepezil hydrochloride, quantity: 5 mg - tablet, film coated - excipient ingredients: magnesium stearate; hyprolose; lactose monohydrate; maize starch; microcrystalline cellulose; hypromellose; macrogol 400; titanium dioxide - arazil (donepezil hydrochloride) is indicated for the treatment of mild, moderate and severe alzheimer?s disease.