SOMATOSTATIN EUMEDICA
3MG INF PSO LQF 1+1ML
SÚKL code | 0200725 |
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Name of the product | SOMATOSTATIN EUMEDICA 3 MG |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | SOMATOSTATIN EUMEDICA |
Supplement | 3MG INF PSO LQF 1+1ML |
Strenght | 3MG |
Pharmaceutical form | Powder and solvent for solution for infusion |
Package | 1+1ML |
Route | Intravenous use |
Wrap type | Ampoule |
Legal status | na lékařský předpis |
Active substance | SOMATOSTATIN (SOMATOSTATINUM) |
ATC group | H01CB01 |
ATC group name | SOMATOSTATIN |
Marketing authorisation information
Registration Number | 56/ 224/93-B/C |
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Type of MA | National |
MA status | B - medicinal product after change, may be placed on the market for the period of 6 months (Placed on the market till) and used until expiration, not later than till the end of validity of the marketing authorisation (Valid till) |
Placed on the market till | 31. 07. 2019 |
MA Holder | Eumedica SA, Brusel |
MA Holder country | BELGIE |
Actual MA holder | EUMEDICA Pharmaceuticals GmbH, Lörrach |
Actual MA holder country | NĚMECKO |