Code | 49780 | ||||||||||
MA number | EU/1/01/190/001 | ||||||||||
Product Form: | plv iol 1x500 IU+1x5 ml solv. (liek.inj.skl.) | ||||||||||
MA Status: | E - Valid centralised marketing authorisation | ||||||||||
Type of procedure: | EU | ||||||||||
MAH, country: | Takeda Manufacturing Austria AG, Austria | ||||||||||
Therapeutic Class: | 75 - SUBSTITUTIO SANGUINIS (A KRVNÉ DERIVÁTY) | ||||||||||
ATC: |
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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 |
MA issued: | 16.07.2001 |
SmPC + PL: |
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Safety feature | Yes |
Data update: | 08.06.2023 |