PREGABALIN LAPL pregabalin 20 mg/mL oral solution bottle

Country: Australia

Language: English

Source: Department of Health (Therapeutic Goods Administration)

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Active ingredient:

pregabalin, Quantity: 20 mg/mL

Available from:

Lupin Australia Pty Limited

INN (International Name):

Pregabalin

Pharmaceutical form:

Oral Liquid, solution

Composition:

Excipient Ingredients: sucralose; monobasic sodium phosphate monohydrate; purified water; dibasic sodium phosphate; propyl hydroxybenzoate; methyl hydroxybenzoate; Flavour

Administration route:

Oral

Units in package:

1

Prescription type:

(S4) Prescription Only Medicine

Therapeutic indications:

Pregabalin LAPL is indicated for the treatment of neuropathic pain in adults. Pregabalin LAPL is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

Product summary:

Visual Identification: A clear colorless liquid with characteristic banana odor.; Container Type: Bottle; Container Material: HDPE; Container Life Time: 6 Months; Container Temperature: Store below 25 degrees Celsius; Container Closure: Child resistant closure

Authorization status:

Licence status A

Authorization date:

2014-12-05