PROSTAPHLIN

1000MG INJ PLV SOL 1

SÚKL code 0092359
Name of the product PROSTAPHLIN 1000 MG
_MA_MEDICATION_DETAIL_INFO_MED_NAME i PROSTAPHLIN
Supplement 1000MG INJ PLV SOL 1
Strenght 1000MG
Pharmaceutical form Powder for solution for injection
Package 1
Route Intravenous use
Language of the pack Czech
Wrap type Vial
Legal status na lékařský předpis
Active substance OXACILLIN SODIUM MONOHYDRATE (OXACILLINUM NATRICUM MONOHYDRICUM)
ATC group J01CF04
ATC group name OXACILIN

Marketing authorisation information

Registration Number 15/ 051/71-S/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 30. 04. 2019
MA Holder Bristol-Myers Squibb spol. s r. o., Praha
MA Holder country ČESKÁ REPUBLIKA
Actual MA holder Laboratoires Delbert, Paříž
Actual MA holder country FRANCIE

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