Lekadol Combo 1000 mg/12,2 mg prašak za oralnu otopinu
Name | Lekadol Combo 1000 mg/12,2 mg prašak za oralnu otopinu |
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Marketing Authorisation Number | HR-H-704869568 |
Active Substance | paracetamol fenilefrinklorid |
Composition | jedna vrećica sadrži 1000 mg paracetamola i 12,2 mg fenilefrinklorida što odgovara 10 mg fenilefrina |
Pharmaceutical Form | Prašak za oralnu otopinu |
Manufacturer | Salutas Pharma GmbH, Barleben, Njemačka Hermes Pharma Ges.m.b.H., Wolfsberg, Austrija |
Marketing Authorisation Holder | Sandoz d.o.o., Maksimirska 120, Zagreb, Hrvatska |
Marketing Authorisation Date | 16.07.2021 |
MA Period of Validity | 16.07.2026 |
Classification Number | UP/I-530-09/21-01/45 |
Registration Number | 381-12-01/70-21-02 |
Prescription | bez recepta |
Distribution | u ljekarni |
Advertising to general public | dopušteno |
ATC Code | N02BE51 |
Medicinal product marketed in the Croatia | Da |
SmPC | download |
PL | download |
Public Assessment Report | download |
Summary of risk management plan | download |