LATANOPROST ACTAVIS
50MCG/ML OPH GTT SOL 3X2,5ML
SÚKL code | 0138510 |
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Name of the product | LATANOPROST ACTAVIS |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | LATANOPROST ACTAVIS |
Supplement | 50MCG/ML OPH GTT SOL 3X2,5ML |
Strenght | 50MCG/ML |
Pharmaceutical form | Eye drops, solution |
Package | 3X2,5ML |
Route | Ocular use |
Language of the pack | Czech |
Wrap type | Dropper container |
Legal status | na lékařský předpis |
Active substance | LATANOPROST (LATANOPROSTUM) |
ATC group | S01EE01 |
ATC group name | LATANOPROST |
Marketing authorisation information
Registration Number | 64/ 501/09-C |
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Type of MA | A mutual recognition procedure (MRP, DCP), where CZ is Reference member state |
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. 05. 2023 |
MA Holder | Actavis Group PTC ehf., Hafnarfjördur |
MA Holder country | ISLAND |
Actual MA holder | Teva B.V., Haarlem |
Actual MA holder country | NIZOZEMSKO |