CHEMMART PREGABALIN pregabalin 100 mg capsule blister pack

Country: Awstralja

Lingwa: Ingliż

Sors: Department of Health (Therapeutic Goods Administration)

Ingredjent attiv:

pregabalin, Quantity: 100 mg

Disponibbli minn:

Arrotex Pharmaceuticals Pty Ltd

INN (Isem Internazzjonali):

Pregabalin

Għamla farmaċewtika:

Capsule, hard

Kompożizzjoni:

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

Rotta amministrattiva:

Oral

Unitajiet fil-pakkett:

56, 20, 14, 60

Tip ta 'preskrizzjoni:

(S4) Prescription Only Medicine

Indikazzjonijiet terapewtiċi:

Pregabalin is indicated for the treatment of neuropathic pain in adults. Pregabalin is also indicated as adjunctive therapy in adults with partial seizures with or without secondary generalization.

Sommarju tal-prodott:

Visual Identification: Capsule with an orange body/orange cap; imprinted with "APO" and "P100" in black ink.; Container Type: Blister Pack; Container Material: PVC/Al; Container Life Time: 24 Months; Container Temperature: Store below 25 degrees Celsius

L-istatus ta 'awtorizzazzjoni:

Registered

Data ta 'l-awtorizzazzjoni:

2012-09-19