Articel-Am 5 mg/5 mg tablete
| Name | Articel-Am 5 mg/5 mg tablete |
|---|---|
| Former Name | Perindopriltosilat/amlodipin Pliva 5 mg/5 mg tablete |
| Marketing Authorisation Number | HR-H-930223952 |
| Active Substance | perindopriltosilat amlodipinbesilat |
| Composition | svaka tableta sadrži 5 mg perindopriltosilata što odgovara 3,4 mg perindoprila i 6,935 mg amlodipinbesilata što odgovara 5 mg amlodipina |
| Pharmaceutical Form | Tableta |
| Manufacturer | Teva Gyogyszergyar Zrt., Debrecen, Mađarska Teva Operations Poland Sp. z o.o., Krakow, Poljska |
| Marketing Authorisation Holder | Pliva Hrvatska d.o.o., Prilaz baruna Filipovića 25, Zagreb, Hrvatska |
| Marketing Authorisation Date | 14.07.2021 |
| MA Period of Validity | 14.07.2026 |
| Classification Number | UP/I-530-09/19-01/307 |
| Registration Number | 381-12-01/70-21-05 |
| Prescription | Medicinal product subject to medical prescription |
| Type of prescription | Medicinal product on medical prescription for renewable delivery |
| Distribution | Supply through pharmacies (community) |
| Advertising to general public | not allowed |
| ATC Code | C09BB04 |
| Marketing status | Marketed |
| Shortage status | No shortage |
| SmPC | download |
| PL | download |
| Public Assessment Report | download |
