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GUTTALAX

5MG TBL NOB 10

SÚKL code 0223130
Name of the product GUTTALAX
_MA_MEDICATION_DETAIL_INFO_MED_NAME i GUTTALAX
Supplement 5MG TBL NOB 10
Strenght 5MG
Pharmaceutical form Tablet
Package 10
Route Oral use
Language of the pack Czech
Wrap type Tablet container
Legal status OTC medicinal products
Active substance SODIUM PICOSULFATE MONOHYDRATE (NATRII PICOSULFAS MONOHYDRICUS)
ATC group A06AB08
ATC group name NATRIUM-PIKOSULFÁT

Marketing authorisation information

Registration Number 61/ 510/05-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. 2021
MA Holder sanofi-aventis, s.r.o., Praha
MA Holder country ČESKÁ REPUBLIKA
Actual MA holder Opella Healthcare Czech s.r.o., Praha
Actual MA holder country ČESKÁ REPUBLIKA

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