PREGABALIN LAPL pregabalin 50 mg capsule blister pack

Country: Ástralía

Tungumál: enska

Heimild: Department of Health (Therapeutic Goods Administration)

Virkt innihaldsefni:

pregabalin, Quantity: 50 mg

Fáanlegur frá:

Lupin Australia Pty Limited

INN (Alþjóðlegt nafn):

Pregabalin

Lyfjaform:

Capsule, hard

Samsetning:

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

Stjórnsýsluleið:

Oral

Einingar í pakka:

20, 14, 56, 60

Gerð lyfseðils:

(S4) Prescription Only Medicine

Ábendingar:

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.

Vörulýsing:

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

Leyfisstaða:

Licence status A

Leyfisdagur:

2014-12-05