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KETOTIFEN AL

1MG CPS DUR 100

SÚKL code 0066002
Name of the product KETOTIFEN AL
_MA_MEDICATION_DETAIL_INFO_MED_NAME i KETOTIFEN AL
Supplement 1MG CPS DUR 100
Strenght 1MG
Pharmaceutical form Capsule, hard
Package 100
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance KETOTIFEN HYDROGEN FUMARATE (KETOTIFENI FUMARAS)
ATC group R06AX17
ATC group name KETOTIFEN

Marketing authorisation information

Registration Number 24/ 509/96-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 28. 02. 2023
MA Holder Aliud Pharma GmbH, Laichingen
MA Holder country NĚMECKO
Actual MA holder STADA Arzneimittel AG, Bad Vilbel
Actual MA holder country NĚMECKO

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