Irbesartan/Hydrochlorothiazide LAPL 150/12.5 irbesartan 150 mg and hydrochlorothiazide 12.5 mg tablet blister pack

Pajjiż: Awstralja

Lingwa: Ingliż

Sors: Department of Health (Therapeutic Goods Administration)

Ixtrih issa

Ingredjent attiv:

irbesartan, Quantity: 150 mg; hydrochlorothiazide, Quantity: 12.5 mg

Disponibbli minn:

Lupin Australia Pty Limited

INN (Isem Internazzjonali):

Hydrochlorothiazide,Irbesartan

Għamla farmaċewtika:

Tablet, film coated

Kompożizzjoni:

Excipient Ingredients: colloidal anhydrous silica; mannitol; magnesium stearate; crospovidone; povidone; poloxamer; titanium dioxide; hypromellose; iron oxide yellow; iron oxide red; macrogol 3350; iron oxide black; propylene glycol; butan-1-ol; isopropyl alcohol; strong ammonia solution; ethanol; Shellac; sulfuric acid

Rotta amministrattiva:

Oral

Unitajiet fil-pakkett:

28 tablets (2 x 14 tablets), 30 tablets (2 x 15 tablets), 56 tablets (4 x 14 tablets), 98 tablets (7 x 14 tablets), 14 tablets (1 x 14 tablets)

Klassi:

Medicine Registered

Tip ta 'preskrizzjoni:

(S4) Prescription Only Medicine

Indikazzjonijiet terapewtiċi:

Irbesartan/HCTZ tablets are indicated for the following:Treatment of hypertension.Treatment should not be initiated with this fixed-dose combination.

Sommarju tal-prodott:

Visual Identification: Light peach, biconvex, oval shaped, film coated tablets, imprinted 'IT1' in black ink on one side and plain on the other side.; Container Type: Blister Pack; Container Material: PVC/PCTFE (Aclar)/Al; Container Life Time: 24 Months; Container Temperature: Store below 25 degrees Celsius

L-istatus ta 'awtorizzazzjoni:

Licence status A

Data ta 'l-awtorizzazzjoni:

2013-06-28