IPCA-AMITRIPTYLINE amitriptyline hydrochloride 10mg tablet blister pack Australia - engelsk - Department of Health (Therapeutic Goods Administration)

ipca-amitriptyline amitriptyline hydrochloride 10mg tablet blister pack

ipca pharma (australia) pty ltd - amitriptyline hydrochloride, quantity: 10 mg - tablet - excipient ingredients: colloidal anhydrous silica; hypromellose; lactose monohydrate; magnesium stearate; crospovidone; macrogol 6000; titanium dioxide; maize starch; microcrystalline cellulose; purified talc; brilliant blue fcf aluminium lake - for the treatment of major depression. amitriptyline 50 mg tablets are indicated only for the maintenance treatment of major depression ,nocturnal enuresis where organic pathology has been excluded.

PIP-AMITRIPTYLINE amitriptyline hydrochloride 25mg tablet bottle pack Australia - engelsk - Department of Health (Therapeutic Goods Administration)

pip-amitriptyline amitriptyline hydrochloride 25mg tablet bottle pack

ipca pharma (australia) pty ltd - amitriptyline hydrochloride, quantity: 25 mg - tablet - excipient ingredients: quinoline yellow aluminium lake; purified talc; colloidal anhydrous silica; macrogol 6000; lactose monohydrate; titanium dioxide; magnesium stearate; microcrystalline cellulose; hypromellose; maize starch; crospovidone - for the treatment of major depression. amitriptyline 50 mg tablets are indicated only for the maintenance treatment of major depression ,nocturnal enuresis where organic pathology has been excluded.

AMIDEP amitriptyline hydrochloride 50mg tablet blister pack Australia - engelsk - Department of Health (Therapeutic Goods Administration)

amidep amitriptyline hydrochloride 50mg tablet blister pack

ipca pharma (australia) pty ltd - amitriptyline hydrochloride, quantity: 50 mg - tablet - excipient ingredients: hypromellose; crospovidone; sunset yellow fcf aluminium lake; maize starch; lactose monohydrate; purified talc; macrogol 6000; magnesium stearate; titanium dioxide; colloidal anhydrous silica; microcrystalline cellulose; indigo carmine aluminium lake - for the treatment of major depression. amitriptyline 50 mg tablets are indicated only for the maintenance treatment of major depression ,nocturnal enuresis where organic pathology has been excluded.

PPA-AMITRIPTYLINE amitriptyline hydrochloride 10mg tablet bottle pack Australia - engelsk - Department of Health (Therapeutic Goods Administration)

ppa-amitriptyline amitriptyline hydrochloride 10mg tablet bottle pack

ipca pharma (australia) pty ltd - amitriptyline hydrochloride, quantity: 10 mg - tablet - excipient ingredients: colloidal anhydrous silica; lactose monohydrate; crospovidone; maize starch; microcrystalline cellulose; titanium dioxide; magnesium stearate; macrogol 6000; purified talc; brilliant blue fcf aluminium lake; hypromellose - for the treatment of major depression. amitriptyline 50 mg tablets are indicated only for the maintenance treatment of major depression ,nocturnal enuresis where organic pathology has been excluded.

ALLERTINE bilastine 20 mg tablet blister pack Australia - engelsk - Department of Health (Therapeutic Goods Administration)

allertine bilastine 20 mg tablet blister pack

a menarini australia pty ltd - bilastine, quantity: 20 mg - tablet, uncoated - excipient ingredients: magnesium stearate; sodium starch glycollate type a; colloidal anhydrous silica; microcrystalline cellulose - for the symptomatic treatment of allergic rhinoconjunctivitis (ar - both seasonal allergic rhinitis (sar) and perennial allergic rhinitis (par)) and/or urticaria.

ADENURIC febuxostat 80 mg tablets blister pack Australia - engelsk - Department of Health (Therapeutic Goods Administration)

adenuric febuxostat 80 mg tablets blister pack

a menarini australia pty ltd - febuxostat, quantity: 80 mg - tablet - excipient ingredients: microcrystalline cellulose; hyprolose; croscarmellose sodium; magnesium stearate; silicon dioxide; lactose monohydrate; titanium dioxide; purified talc; iron oxide yellow; polyvinyl alcohol; macrogol 3350 - treatment of chronic symptomatic hyperuricaemia in conditions where urate deposition has already occurred (gouty arthritis and/or tophus formation) in adults with gout.