PREGABALIN LAPL pregabalin 50 mg capsule blister pack

Land: Australië

Taal: Engels

Bron: Department of Health (Therapeutic Goods Administration)

Werkstoffen:

pregabalin, Quantity: 50 mg

Beschikbaar vanaf:

Lupin Australia Pty Limited

INN (Algemene Internationale Benaming):

Pregabalin

farmaceutische vorm:

Capsule, hard

Samenstelling:

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

Toedieningsweg:

Oral

Eenheden in pakket:

20, 14, 56, 60

Prescription-type:

(S4) Prescription Only Medicine

therapeutische indicaties:

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.

Product samenvatting:

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

Autorisatie-status:

Licence status A

Autorisatie datum:

2014-12-05