| Code | 41663 | ||||||||||
| MA number | EU/1/02/226/001 | ||||||||||
| Product Form: | kit imp 1x12 mg (1 skl.liek.-powder+1 skl.liek.-solv.+1 matrix+2 striek.+2 ih.) | ||||||||||
| MA Status: | E - Valid centralised marketing authorisation | ||||||||||
| Type of procedure: | EU | ||||||||||
| MAH, country: | Medtronic BioPharma B.V., Netherland | ||||||||||
| Therapeutic Class: | 87 - VARIA I | ||||||||||
| ATC: |
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| Shelf life: | 36 | ||||||||||
| Container: | glass vial | ||||||||||
| Route of admin.: | Osseous use |
| Prescription Status: | Medicinal product subject to medical prescription. |
| Legal basis: | Article 8(3) application |
| MA issued: | 09.09.2002 |
| SmPC + PL: |
European Medicines Agency's database
|
| Safety feature | Yes |
| Data update: | 18.06.2018 |
