PREGABALIN LAPL pregabalin 300 mg capsule blister pack

Země: Austrálie

Jazyk: angličtina

Zdroj: Department of Health (Therapeutic Goods Administration)

Aktivní složka:

pregabalin, Quantity: 300 mg

Dostupné s:

Lupin Australia Pty Limited

INN (Mezinárodní Name):

Pregabalin

Léková forma:

Capsule, hard

Složení:

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

Podání:

Oral

Jednotky v balení:

20, 60, 14, 56

Druh předpisu:

(S4) Prescription Only Medicine

Terapeutické indikace:

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.

Přehled produktů:

Visual Identification: Size '0' capsules with dark brown cap and white body, imprinted with "PG" on cap and "300" on 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

Stav Autorizace:

Licence status A

Datum autorizace:

2014-12-05