| Code | 5581C | ||||||||||
| MA number | EU/1/17/1214/001 | ||||||||||
| Product Form: | con inf 1x10 ml/200 mg (liek.inj.skl.) | ||||||||||
| MA Status: | E - Valid centralised marketing authorisation | ||||||||||
| Type of procedure: | EU | ||||||||||
| MAH, country: | Merck Europe B.V., Netherland | ||||||||||
| Therapeutic Class: | 44 - CYTOSTATICA | ||||||||||
| ATC: |
|
||||||||||
| Shelf life: | 36 | ||||||||||
| Container: | glass vial | ||||||||||
| Route of admin.: | Intravenous use |
| Prescription Status: | Medicinal product subject to restricted medical prescription. |
| Legal basis: | Article 8(3) application - new active substance |
| MA issued: | 19.08.2020 |
| SmPC + PL: |
European Medicines Agency's database
|
| Dokument: |
Bavencio_Karta pacienta.pdf
|
| Dokument: |
Bavencio_Prirucka pre zdravotnickych pracovnikov.pdf
|
| Dokument: |
Bavencio_Prirucka pre pacientov.pdf
|
| Safety feature | Yes |
| Data update: | 23.03.2025 |
