New Zealand - English - Medsafe (Medicines Safety Authority)

pharmacy retailing (nz) ltd t/a healthcare logistics - nicorandil 20mg - tablet - 20 mg - active: nicorandil 20mg excipient: croscarmellose sodium maize starch mannitol stearic acid - nicorandil is indicated for the symptomatic treatment of stable angina pectoris that is inadequately controlled or have a contraindication or intolerance to first-line anti-anginal therapies.

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

sanofi-aventis australia pty ltd - nicorandil -

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

a menarini australia pty ltd - dapoxetine hydrochloride -

New Zealand - English - Medsafe (Medicines Safety Authority)

a. menarini new zealand pty ltd - dapoxetine hydrochloride 33.6mg equivalent to dapoxetine 30 mg;   - film coated tablet - 30 mg - active: dapoxetine hydrochloride 33.6mg equivalent to dapoxetine 30 mg   excipient: colloidal silicon dioxide croscarmellose sodium coating powder grey 4 lactose monohydrate as a spray-dried mixture of lactose monohydrate & microcrystalline cellulose magnesium stearate microcrystalline cellulose as a spray-dried mixture of lactose monohydrate & microcrystalline cellulose - priligy is indicated for the treatment of premature ejaculation (pe) in men 18 to 64 years of age, who have all of the following: · persistent or recurrent ejaculation with minimal sexual stimulation before, on, or shortly after penetration and before the patient wishes; and · marked personal distress or interpersonal difficulty as a consequence of pe; and · poor control over ejaculation.

New Zealand - English - Medsafe (Medicines Safety Authority)

a. menarini new zealand pty ltd - dapoxetine hydrochloride 67.2mg equivalent to dapoxetine 60 mg;   - film coated tablet - 60 mg - active: dapoxetine hydrochloride 67.2mg equivalent to dapoxetine 60 mg   excipient: colloidal silicon dioxide croscarmellose sodium coating powder grey 3 lactose monohydrate as a spray-ried mixture of lactose monohydrate & microcrystalline cellulose magnesium stearate microcrystalline cellulose as a spray-ried mixture of lactose monohydrate & microcrystalline cellulose - priligy is indicated for the treatment of premature ejaculation (pe) in men 18 to 64 years of age, who have all of the following: · persistent or recurrent ejaculation with minimal sexual stimulation before, on, or shortly after penetration and before the patient wishes; and · marked personal distress or interpersonal difficulty as a consequence of pe; and · poor control over ejaculation.

Canada - English - Health Canada

paladin labs inc. - doxepin (doxepin hydrochloride) - tablet - 3mg - doxepin (doxepin hydrochloride) 3mg - tricyclics and other norepinephrine-reuptake inhibitors

Canada - English - Health Canada

paladin labs inc. - doxepin (doxepin hydrochloride) - tablet - 6mg - doxepin (doxepin hydrochloride) 6mg - tricyclics and other norepinephrine-reuptake inhibitors

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

arrotex pharmaceuticals pty ltd - nicorandil, quantity: 10 mg - tablet, uncoated - excipient ingredients: povidone; cetyl alcohol; croscarmellose sodium; sodium stearylfumarate; mannitol - nicorandil is indicated for the treatment of chronic stable angina pectoris.

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

arrotex pharmaceuticals pty ltd - nicorandil, quantity: 20 mg - tablet, uncoated - excipient ingredients: croscarmellose sodium; mannitol; povidone; cetyl alcohol; sodium stearylfumarate - nicorandil is indicated for the treatment of chronic stable angina pectoris.

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

sanofi-aventis australia pty ltd - nicorandil, quantity: 20 mg - tablet, uncoated - excipient ingredients: maize starch; stearic acid; mannitol; croscarmellose sodium - ikorel is indicated for the treatment of chronic stable angina pectoris.