| Code | 50539 | ||||||||||
| MA number | EU/1/00/143/010 | ||||||||||
| Product Form: | plv iol 1x2000 IU (1x skl. liek.- powder+1x skl.napln.striek.-solv.+1x Bio-Set device) | ||||||||||
| MA Status: | E - Valid centralised marketing authorisation | ||||||||||
| Type of procedure: | EU | ||||||||||
| MAH, country: | Bayer AG, Germany | ||||||||||
| Therapeutic Class: | 75 - SUBSTITUTIO SANGUINIS (A KRVNÉ DERIVÁTY) | ||||||||||
| ATC: |
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| Shelf life: | 30 | ||||||||||
| Container: | glass vial | ||||||||||
| Route of admin.: | Intravenous use |
| Prescription Status: | Medicinal product subject to restricted medical prescription. |
| Legal basis: | Article 8(3) application |
| MA issued: | 18.12.2007 |
| SmPC + PL: |
European Medicines Agency's database
|
| Safety feature | Yes |
| Data update: | 18.06.2018 |
