PREGABALIN LAPL pregabalin 50 mg capsule blister pack

Country: Australia

Bahasa: Inggeris

Sumber: Department of Health (Therapeutic Goods Administration)

Beli sekarang

Laporan Penilaian Awam Laporan Penilaian Awam (PAR)
26-11-2017

Bahan aktif:

pregabalin, Quantity: 50 mg

Boleh didapati daripada:

Lupin Australia Pty Limited

INN (Nama Antarabangsa):

Pregabalin

Borang farmaseutikal:

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

Laluan pentadbiran:

Oral

Unit dalam pakej:

20, 14, 56, 60

Jenis preskripsi:

(S4) Prescription Only Medicine

Tanda-tanda terapeutik:

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 kebenaran:

Licence status A

Tarikh kebenaran:

2014-12-05