Code | 0817E | ||||||||||
MA number | EU/1/19/1413/002 | ||||||||||
Product Form: | plv inu 1x150 mg (liek.inj.skl.) | ||||||||||
MA Status: | E - Valid centralised marketing authorisation | ||||||||||
Type of procedure: | EU | ||||||||||
Therapeutic Class: | 44 - CYTOSTATICA | ||||||||||
ATC: |
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Shelf life: | 36 | ||||||||||
Container: | glass vial | ||||||||||
Route of admin.: | Subcutaneous use |
Prescription Status: | Medicinal product subject to restricted medical prescription. |
Legal basis: | Article 10(1) generic application |
MA issued: | 13.02.2020 |
Validity: | 13.02.2025 |
SmPC + PL: |
|
Safety feature | Yes |
Data update: | 15.05.2022 |