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SEFOTAK

1G INJ/INF PLV SOL 1

SÚKL code 0201030
Name of the product SEFOTAK
_MA_MEDICATION_DETAIL_INFO_MED_NAME i SEFOTAK
Supplement 1G INJ/INF PLV SOL 1
Strenght 1G
Pharmaceutical form Powder for solution for injection/infusion
Package 1
Route Intramuscular/intravenous use
Language of the pack Czech
Wrap type Vial
Legal status na lékařský předpis
Active substance CEFOTAXIME SODIUM (CEFOTAXIMUM NATRICUM)
ATC group J01DD01
ATC group name CEFOTAXIM

Marketing authorisation information

Registration Number 15/ 611/99-C
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. 12. 2020
MA Holder PharmaSwiss Česká republika s.r.o., Praha
MA Holder country ČESKÁ REPUBLIKA
Actual MA holder Bausch Health Ireland Limited, Dublin
Actual MA holder country IRSKO

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