| Code | 6232E | ||||||||||
| MA number | 16/0113/24-S | ||||||||||
| Product Form: | tbl flm 30x500 mg (blis.Al/PVC/PVDC) | ||||||||||
| MA Status: | R - Valid Marketing Authorisation | ||||||||||
| Type of procedure: | Decentralised | ||||||||||
| MAH, country: | MAKPHARM d.o.o., Croatia | ||||||||||
| Therapeutic Class: | 16 - ANTICOAGULANTIA (FIBRINOLYTICA, ANTIFIBRINOL.) | ||||||||||
| ATC: |
|
||||||||||
| Shelf life: | 30 | ||||||||||
| Container: | blister Al/PVC/PVDC | ||||||||||
| Route of admin.: | Oral use |
| Prescription Status: | Medicinal product subject to medical prescription. |
| Legal basis: | Article 10(1) generic application |
| MA issued: | 21.05.2024 |
| Validity: | 21.05.2029 |
| Pediatric indication: | Yes |
| Pediatric posology: | Yes |
| Pediatric warnings: | Yes |
| PIL: |
PIL_Trenolk 500 mg filmom obalené tablety_05_2024.pdf
|
| SPC: |
SPC_Trenolk 500 mg filmom obalené tablety_05_2024.pdf
|
| Safety feature | Yes |
| Data update: | 22.05.2024 |
