| Code | 21434 | ||||||||||
| MA number | 05/0403/10-S | ||||||||||
| Product Form: | plc ifu 5x1 mg (liek.inj.skl.) | ||||||||||
| MA Status: | D - Marketing Authorisation valid for an unlimited period | ||||||||||
| Type of procedure: | Mutual recognition procedure | ||||||||||
| MAH, country: | B.Braun Melsungen AG, Germany | ||||||||||
| Therapeutic Class: | 05 - ANAESTHETICA (CELKOVÉ) | ||||||||||
| ATC: |
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| Shelf life: | 24 | ||||||||||
| Container: | glass vial | ||||||||||
| Route of admin.: | Intravenous use |
| Prescription Status: | Medicinal product subject to special medical prescription with skew blue stripe. |
| Legal basis: | Article 10(1) generic application |
| MA issued: | 22.07.2010 |
| Pediatric posology: | Yes |
| Pediatric warnings: | Yes |
| SPC: |
SPC_Remifentanil BBraun_08_2022.pdf
|
| PIL: |
PIL_Remifentanil BBraun_ 08_2022.pdf
|
| Safety feature | Yes |
| Data update: | 21.10.2019 |
