| Code | 93959 | ||||
| MA number | 88/0158/04-S | ||||
| Product Form: | kit 5x0,5 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 |
