PREGABALIN LAPL pregabalin 50 mg capsule blister pack

Negara: Australia

Bahasa: Inggris

Sumber: Department of Health (Therapeutic Goods Administration)

Bahan aktif:

pregabalin, Quantity: 50 mg

Tersedia dari:

Lupin Australia Pty Limited

INN (Nama Internasional):

Pregabalin

Bentuk farmasi:

Capsule, hard

Komposisi:

Excipient Ingredients: pregelatinised maize starch; purified talc; titanium dioxide; purified water; Gelatin; sodium lauryl sulfate; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; Shellac; strong ammonia solution; iron oxide black; potassium hydroxide; ethanol absolute

Rute administrasi :

Oral

Unit dalam paket:

20, 14, 56, 60

Jenis Resep:

(S4) Prescription Only Medicine

Indikasi Terapi:

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.

Ringkasan produk:

Visual Identification: Size '4' capsules with white cap and white body, imprinted with "PG" on the cap and with a band and with "50" on the body in black ink, containing white to off white powder; Container Type: Blister Pack; Container Material: PVC/Al; Container Life Time: 24 Months; Container Temperature: Store below 25 degrees Celsius; Container Closure: Neither child resistant closure nor restricted flow insert

Status otorisasi:

Licence status A

Tanggal Otorisasi:

2014-12-05