PREGABALIN LAPL pregabalin 20 mg/mL oral solution bottle

Ülke: Avustralya

Dil: İngilizce

Kaynak: Department of Health (Therapeutic Goods Administration)

Aktif bileşen:

pregabalin, Quantity: 20 mg/mL

Mevcut itibaren:

Lupin Australia Pty Limited

INN (International Adı):

Pregabalin

Farmasötik formu:

Oral Liquid, solution

Kompozisyon:

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

Uygulama yolu:

Oral

Paketteki üniteler:

1

Reçete türü:

(S4) Prescription Only Medicine

Terapötik endikasyonlar:

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.

Ürün özeti:

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

Yetkilendirme durumu:

Licence status A

Yetkilendirme tarihi:

2014-12-05