DESVENLAFAXINE EXTENDED-RELEASE- desvenlafaxine tablet, extended release United States - English - NLM (National Library of Medicine)

desvenlafaxine extended-release- desvenlafaxine tablet, extended release

macoven pharmaceuticals - desvenlafaxine (unii: ng99554anw) (desvenlafaxine - unii:ng99554anw) - desvenlafaxine 50 mg - desvenlafaxine extended-release tablets are indicated for the treatment of adults with major depressive disorder (mdd) [see clinical studies (14)] . - hypersensitivity to desvenlafaxine succinate, venlafaxine hydrochloride or to any excipients in the desvenlafaxine extended-release tablets formulation.  angioedema has been reported in patients treated with desvenlafaxine [see adverse reactions (6.1)] . - the use of maois intended to treat psychiatric disorders with desvenlafaxine extended-release tablets or within 7 days of stopping treatment with desvenlafaxine extended-release tablets is contraindicated because of an increased risk of serotonin syndrome. the use of desvenlafaxine extended-release tablets within 14 days of stopping an maoi intended to treat psychiatric disorders is also contraindicated [see dosage and administration  (2.8)   and  warnings and precautions  (5.2)]. -   starting desvenlafaxine extended-release tablets in a patient who is being treated with maois such as linezolid or intraveno

VENLAFAXINE GENERICHEALTH XR venlafaxine (as hydrochloride) 75mg modified release capsule blister Australia - English - Department of Health (Therapeutic Goods Administration)

venlafaxine generichealth xr venlafaxine (as hydrochloride) 75mg modified release capsule blister

generic health pty ltd - venlafaxine hydrochloride, quantity: 84.86 mg - capsule, modified release - excipient ingredients: hypromellose; magnesium stearate; sodium lauryl sulfate; ammonio methacrylate copolymer; basic butylated methacrylate copolymer; titanium dioxide; iron oxide red; potable water; gelatin - treatment of major depression, including prevention of relapse and recurrence where appropriate; generalised anxiety disorder; social anxiety disorder; and panic disorder, including prevention of relapse.

VENLAFAXINE GENERICHEALTH XR venlafaxine (as hydrochloride) 150mg modified release capsule blister Australia - English - Department of Health (Therapeutic Goods Administration)

venlafaxine generichealth xr venlafaxine (as hydrochloride) 150mg modified release capsule blister

generic health pty ltd - venlafaxine hydrochloride, quantity: 169.71 mg - capsule, modified release - excipient ingredients: magnesium stearate; hypromellose; ammonio methacrylate copolymer; sodium lauryl sulfate; basic butylated methacrylate copolymer; titanium dioxide; indigo carmine; erythrosine; potable water; gelatin - treatment of major depression, including prevention of relapse and recurrence where appropriate; generalised anxiety disorder; social anxiety disorder; and panic disorder, including prevention of relapse.

DESVENLAFAXINE GH XR  desvenlafaxine (as benzoate) 100 mg extended release tablets blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

desvenlafaxine gh xr desvenlafaxine (as benzoate) 100 mg extended release tablets blister pack

lupin australia pty limited - desvenlafaxine benzoate, quantity: 146.32 mg (equivalent: desvenlafaxine, qty 100 mg) - tablet, modified release - excipient ingredients: hypromellose; colloidal anhydrous silica; purified talc; microcrystalline cellulose; stearic acid; titanium dioxide; sunset yellow fcf aluminium lake; iron oxide red; polyvinyl alcohol; macrogol 3350 - desvenlafaxine is indicated for the treatment of major depressive disorder, including the prevention of relapse.,desvenlafaxine is not indicated for paediatric use.

DESVENLAFAXINE GH XR  desvenlafaxine (as benzoate) 50 mg extended release tablets blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

desvenlafaxine gh xr desvenlafaxine (as benzoate) 50 mg extended release tablets blister pack

lupin australia pty limited - desvenlafaxine benzoate, quantity: 73.16 mg (equivalent: desvenlafaxine, qty 50 mg) - tablet, modified release - excipient ingredients: hypromellose; colloidal anhydrous silica; purified talc; microcrystalline cellulose; stearic acid; titanium dioxide; iron oxide yellow; iron oxide red; polyvinyl alcohol; macrogol 3350 - desvenlafaxine is indicated for the treatment of major depressive disorder, including the prevention of relapse.,desvenlafaxine is not indicated for paediatric use.