Code | 40737 | ||||||||||
MA number | EU/1/00/169/005 | ||||||||||
Product Form: | plv iol 1x40 mg/8 KU + 1x8 ml solv. (liek.inj.skl. + striek.inj.napl.plast) | ||||||||||
MA Status: | E - Valid centralised marketing authorisation | ||||||||||
Type of procedure: | EU | ||||||||||
MAH, country: | Boehringer Ingelheim International GmbH, Germany | ||||||||||
Therapeutic Class: | 16 - ANTICOAGULANTIA (FIBRINOLYTICA, ANTIFIBRINOL.) | ||||||||||
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 |
MA issued: | 23.02.2001 |
SmPC + PL: | European Medicines Agency's database |
Safety feature | Yes |
Data update: | 26.01.2024 |