KETOTIFEN AL
1MG CPS DUR 100
SÚKL code | 0066002 |
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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 |
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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 |