Code | 2182E | ||||||
MA number | EU/1/22/1680/006 | ||||||
Product Form: | pra ras 3x10 ml (liek.inj.skl.) | ||||||
MA Status: | E - Valid centralised marketing authorisation | ||||||
Type of procedure: | EU | ||||||
MAH, country: | Billev Pharma ApS, Denmark | ||||||
Therapeutic Class: | 88 - RADIOPHARMACA | ||||||
ATC: |
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Shelf life: | 11 dní | ||||||
Container: | glass vial | ||||||
Route of admin.: | Route of administration not applicable |
Prescription Status: | Medicinal product subject to medical prescription. |
Legal basis: | Article 10a well-established use application |
MA issued: | 15.09.2022 |
Validity: | 15.09.2027 |
SmPC + PL: | European Medicines Agency's database |
Safety feature | Yes |
Data update: | 20.11.2023 |