PRODUCT DETAIL

Bevimlar 15 mg filmom obalené tablety + Bevimlar 20 mg filmom obalené tablety

Code

4114E

MA number

16/0172/23-S

Product Form:

tbl flm 49(42x1x15 mg+7x1x20 mg) (blis.PVC/PVDC/Al-jednotliv.dáv.)

MA Status:

R - Valid Marketing Authorisation

Type of procedure:

Decentralised

Therapeutic Class:

16 - ANTICOAGULANTIA (FIBRINOLYTICA, ANTIFIBRINOL.)

ATC:

B	BLOOD AND BLOOD FORMING ORGANS
B01	ANTITHROMBOTIC AGENTS
B01A	ANTITHROMBOTIC AGENTS
B01AF	Direct factor Xa inhibitors
B01AF01	Rivaroxaban

Shelf life:

Container:

blister PVC/PVDC/Al

Route of admin.:

Oral use

Prescription Status:	Medicinal product subject to medical prescription.
Legal basis:	Article 10(1) generic application
MA issued:	10.08.2023
Validity:	10.08.2028
PIL:	PIL_Bevimlar 15 mg filmom obalené tablety + Bevimlar 20 mg filmom obalené tablety_07_2023.pdf
SPC:	SPC_Bevimlar 15 mg filmom obalené tablety + Bevimlar 20 mg filmom obalené tablety_07_2023.pdf
Safety feature	Yes
Data update:	14.08.2023