ISOSORBIDE MONONITRATE tablet, extended release Statele Unite ale Americii - engleză - NLM (National Library of Medicine)

isosorbide mononitrate tablet, extended release

torrent pharmaceuticals limited - isosorbide mononitrate (unii: lx1oh63030) (isosorbide mononitrate - unii:lx1oh63030) - isosorbide mononitrate 30 mg - isosorbide mononitrate extended-release tablets are indicated for the prevention of angina pectoris due to coronary artery disease. the onset of action of oral isosorbide mononitrate is not sufficiently rapid for this product to be useful in aborting an acute anginal episode. isosorbide mononitrate extended-release tablets are contraindicated in patients who have shown hypersensitivity or idiosyncratic reactions to other nitrates or nitrites.

ISOSORBIDE MONONITRATE tablet, extended release Statele Unite ale Americii - engleză - NLM (National Library of Medicine)

isosorbide mononitrate tablet, extended release

lannett company, inc. - isosorbide mononitrate (unii: lx1oh63030) (isosorbide mononitrate - unii:lx1oh63030) - isosorbide mononitrate 30 mg - isosorbide mononitrate extended-release tablets are indicated for the prevention of angina pectoris due to coronary artery disease. the onset of action of oral isosorbide mononitrate is not sufficiently rapid for this product to be useful in aborting an acute anginal episode. isosorbide mononitrate extended-release tablets are contraindicated in patients who have shown hypersensitivity or idiosyncratic reactions to other nitrates or nitrites.

ISOSORBIDE MONONITRATE- isosorbide mononitrate tablet, extended release Statele Unite ale Americii - engleză - NLM (National Library of Medicine)

isosorbide mononitrate- isosorbide mononitrate tablet, extended release

par pharmaceutical - isosorbide mononitrate (unii: lx1oh63030) (isosorbide mononitrate - unii:lx1oh63030) - isosorbide mononitrate 30 mg - isosorbide mononitrate extended-release tablets are indicated for the prevention of angina pectoris due to coronary artery disease. the onset of action of oral isosorbide mononitrate is not sufficiently rapid for this product to be useful in aborting an acute anginal episode. isosorbide mononitrate extended-release tablets are contraindicated in patients who have shown hypersensitivity or idiosyncratic reactions to other nitrates or nitrites.

SIFROL ER pramipexole dihydrochloride monohydrate 4.5 mg extended-release tablet blister pack Australia - engleză - Department of Health (Therapeutic Goods Administration)

sifrol er pramipexole dihydrochloride monohydrate 4.5 mg extended-release tablet blister pack

boehringer ingelheim pty ltd - pramipexole dihydrochloride monohydrate, quantity: 4.5 mg - tablet, modified release - excipient ingredients: colloidal anhydrous silica; hypromellose; maize starch; carbomer 941; magnesium stearate - for the treatment of signs and symptoms of idiopathic parkinson's disease. it may be used as monotherapy or in combination with levodopa.

SIFROL ER pramipexole dihydrochloride monohydrate 3 mg extended-release tablet blister pack Australia - engleză - Department of Health (Therapeutic Goods Administration)

sifrol er pramipexole dihydrochloride monohydrate 3 mg extended-release tablet blister pack

boehringer ingelheim pty ltd - pramipexole dihydrochloride monohydrate, quantity: 3 mg - tablet, modified release - excipient ingredients: maize starch; hypromellose; colloidal anhydrous silica; carbomer 941; magnesium stearate - for the treatment of signs and symptoms of idiopathic parkinson's disease. it may be used as monotherapy or in combination with levodopa.

SIFROL ER  pramipexole dihydrochloride monohydrate 1.5 mg extended-release tablet blister pack Australia - engleză - Department of Health (Therapeutic Goods Administration)

sifrol er pramipexole dihydrochloride monohydrate 1.5 mg extended-release tablet blister pack

boehringer ingelheim pty ltd - pramipexole dihydrochloride monohydrate, quantity: 1.5 mg - tablet, modified release - excipient ingredients: colloidal anhydrous silica; magnesium stearate; maize starch; hypromellose; carbomer 941 - for the treatment of signs and symptoms of idiopathic parkinson's disease. it may be used as monotherapy or in combination with levodopa.

SIFROL ER pramipexole dihydrochloride monohydrate 0.75 mg extended-release tablet blister pack Australia - engleză - Department of Health (Therapeutic Goods Administration)

sifrol er pramipexole dihydrochloride monohydrate 0.75 mg extended-release tablet blister pack

boehringer ingelheim pty ltd - pramipexole dihydrochloride monohydrate, quantity: 0.75 mg - tablet, modified release - excipient ingredients: maize starch; colloidal anhydrous silica; hypromellose; carbomer 941; magnesium stearate - for the treatment of signs and symptoms of idiopathic parkinson's disease. it may be used as monotherapy or in combination with levodopa.

SIFROL ER  pramipexole dihydrochloride monohydrate 0.375 mg extended-release tablet blister pack Australia - engleză - Department of Health (Therapeutic Goods Administration)

sifrol er pramipexole dihydrochloride monohydrate 0.375 mg extended-release tablet blister pack

boehringer ingelheim pty ltd - pramipexole dihydrochloride monohydrate, quantity: 0.375 mg - tablet, modified release - excipient ingredients: maize starch; hypromellose; magnesium stearate; colloidal anhydrous silica; carbomer 941 - for the treatment of signs and symptoms of idiopathic parkinson's disease. it may be used as monotherapy or in combination with levodopa.

ISOSORBIDE MONONITRATE tablet Statele Unite ale Americii - engleză - NLM (National Library of Medicine)

isosorbide mononitrate tablet

remedyrepack inc. - isosorbide mononitrate (unii: lx1oh63030) (isosorbide mononitrate - unii:lx1oh63030) - isosorbide mononitrate 30 mg - isosorbide mononitrate extended-release tablets are indicated for the prevention of angina pectoris due to coronary artery disease. the onset of action of oral ismn is not sufficiently rapid for this product to be useful in aborting an acute angina episode. isosorbide mononitrate extended-release tablets are contraindicated in patients who have shown hypersensitivity or idiosyncratic reactions to other nitrates or nitrites.

DONEPEZIL SANDOZ donepezil hydrochloride (as monohydrate) 5mg film-coated tablet blister pack Australia - engleză - Department of Health (Therapeutic Goods Administration)

donepezil sandoz donepezil hydrochloride (as monohydrate) 5mg film-coated tablet blister pack

sandoz pty ltd - donepezil hydrochloride monohydrate, quantity: 5.22 mg (equivalent: donepezil hydrochloride, qty 5 mg) - tablet, film coated - excipient ingredients: lactose monohydrate; microcrystalline cellulose; magnesium stearate; maize starch; titanium dioxide; purified talc; polyvinyl alcohol; macrogol 3350; lecithin - treatment of mild, moderate and severe alzheimer's disease.