DESVENLAFAXINE MEDIS desvenlafaxine 50mg modified release tablets blister

Country: Australia

Language: English

Source: Department of Health (Therapeutic Goods Administration)

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Active ingredient:

desvenlafaxine, Quantity: 50 mg

Available from:

Medis Pharma Pty Ltd

INN (International Name):

Desvenlafaxine

Pharmaceutical form:

Tablet, modified release

Composition:

Excipient Ingredients: microcrystalline cellulose; citric acid monohydrate; hypromellose; alginic acid; purified talc; magnesium stearate; povidone; titanium dioxide; macrogol 6000; iron oxide red

Administration route:

Oral

Units in package:

28, 14, 7

Prescription type:

(S4) Prescription Only Medicine

Therapeutic indications:

For the treatment of major depressive disorder, including the preventiton of relapse. Not indicated for paediatric use.

Product summary:

Visual Identification: Light pink colored, diamond shaped, biconvex tablets, debossed with 'Ll89' on one side and plain on other side.; Container Type: Blister Pack; Container Material: PVC/PVDC/Al; Container Life Time: 4 Years; Container Temperature: Store below 25 degrees Celsius; Container Closure: Neither child resistant closure nor restricted flow insert

Authorization status:

Licence status A

Authorization date:

2014-11-26