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VANCOMYCIN MYLAN

500MG INF PLV SOL 20

SÚKL code 0166268
Name of the product VANCOMYCIN MYLAN
_MA_MEDICATION_DETAIL_INFO_MED_NAME i VANCOMYCIN MYLAN
Supplement 500MG INF PLV SOL 20
Strenght 500MG
Pharmaceutical form Powder for solution for infusion
Package 20
Route Intravenous/oral use
Language of the pack Czech
Wrap type Vial
Legal status na lékařský předpis
Active substance VANCOMYCIN HYDROCHLORIDE (VANCOMYCINI HYDROCHLORIDUM)
ATC group J01XA01
ATC group name VANKOMYCIN

Marketing authorisation information

Registration Number 15/ 354/11-C
Type of MA A mutual recognition procedure (MRP, DCP), where CZ is Reference member state
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. 05. 2022
MA Holder Mylan S.A.S., Saint-Priest
MA Holder country FRANCIE
Actual MA holder VIATRIS LIMITED, Dublin
Actual MA holder country IRSKO

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