DOLIRIEF
400MG TBL FLM 10 II
SÚKL code | 0207872 |
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Name of the product | DOLIRIEF |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | DOLIRIEF |
Supplement | 400MG TBL FLM 10 II |
Strenght | 400MG |
Pharmaceutical form | Film-coated tablet |
Package | 10 II |
Route | Oral use |
Language of the pack | Czech |
Wrap type | Blister |
Legal status | OTC medicinal products |
Active substance | IBUPROFEN LYSINE (IBUPROFENUM LYSINICUM) |
ATC group | M01AE01 |
ATC group name | IBUPROFEN |
Marketing authorisation information
Registration Number | 29/1047/16-C |
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Type of MA | A mutual recognition procedure (MRP, DCP), where CZ is Concerned member state |
MA status | R - active MA/authorised medicinal product |
MA Holder | Alkaloid - INT d.o.o., Ljubljana - Črnuče |
MA Holder country | SLOVINSKO |