PREGABALIN LAPL pregabalin 50 mg capsule blister pack

Χώρα: Αυστραλία

Γλώσσα: Αγγλικά

Πηγή: Department of Health (Therapeutic Goods Administration)

Δραστική ουσία:

pregabalin, Quantity: 50 mg

Διαθέσιμο από:

Lupin Australia Pty Limited

INN (Διεθνής Όνομα):

Pregabalin

Φαρμακοτεχνική μορφή:

Capsule, hard

Σύνθεση:

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

Οδός χορήγησης:

Oral

Μονάδες σε πακέτο:

20, 14, 56, 60

Τρόπος διάθεσης:

(S4) Prescription Only Medicine

Θεραπευτικές ενδείξεις:

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.

Περίληψη προϊόντος:

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

Καθεστώς αδειοδότησης:

Licence status A

Ημερομηνία της άδειας:

2014-12-05