Code | 93958 | ||||
MA number | 88/0158/04-S | ||||
Product Form: | kit 2x0,5 mg (liek.inj.skl.) | ||||
MA Status: | D - Marketing Authorisation valid for an unlimited period | ||||
Type of procedure: | National | ||||
MAH, country: | GE Healthcare AS, Norway | ||||
Therapeutic Class: | 88 - RADIOPHARMACA | ||||
ATC: |
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Shelf life: | 52 týždňov | ||||
Container: | glass vial | ||||
Route of admin.: | Intravenous use |
Prescription Status: | Medicinal product subject to medical prescription. |
Legal basis: | Article 8(3) application - known active substance |
MA issued: | 30.04.2004 |
Pediatric warnings: | Yes |
PIL: | PIL_Ceretec_03.2019.doc |
SPC: | SPC_Ceretec_11.2022.pdf |
Safety feature | No |
Data update: | 17.10.2019 |