Lekadol Combo 1000 mg/12,2 mg prašak za oralnu otopinu
| Name | Lekadol Combo 1000 mg/12,2 mg prašak za oralnu otopinu |
|---|---|
| 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 | Medicinal product not subject to medical prescription |
| Distribution | Supply through pharmacies (community) |
| Advertising to general public | allowed |
| ATC Code | N02BE51 |
| Marketing status | stavljeno u promet |
| Shortage status | nema nestašice |
| SmPC | download |
| PL | download |
| Public Assessment Report | download |
| Summary of risk management plan | download |
