CIPLOX

500MG TBL FLM 200

SÚKL code 0015660
Name of the product CIPLOX
_MA_MEDICATION_DETAIL_INFO_MED_NAME i CIPLOX
Supplement 500MG TBL FLM 200
Strenght 500MG
Pharmaceutical form Film-coated tablet
Package 200
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance CIPROFLOXACIN HYDROCHLORIDE MONOHYDRATE (CIPROFLOXACINI HYDROCHLORIDUM MONOHYDRICUM)
ATC group J01MA02
ATC group name CIPROFLOXACIN

Marketing authorisation information

Registration Number 42/1237/97-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. 07. 2019
MA Holder Cipla (UK) Limited, Addlestone
MA Holder country VELKÁ BRITÁNIE
Actual MA holder Cipla Europe NV, Antverpy
Actual MA holder country BELGIE

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