Symbicort 80 mikrograma/2,25 mikrograma po potisku, stlačeni inhalat, suspenzija
| Name | Symbicort 80 mikrograma/2,25 mikrograma po potisku, stlačeni inhalat, suspenzija |
|---|---|
| Marketing Authorisation Number | HR-H-885448176 |
| Active Substance | budezonid formoterolfumarat dihidrat |
| Composition | Jedna isporučena doza (iz aktivatora) sadrži 80 mikrograma budezonida i 2,25 mikrograma formoterolfumarat dihidrata po potisku |
| Pharmaceutical Form | stlačeni inhalat, suspenzija |
| Manufacturer | AstraZeneca Dunkerque Production, Dunkerque, Francuska |
| Marketing Authorisation Holder | AstraZeneca d.o.o., Ulica Vjekoslava Heinzela 70, Zagreb, Hrvatska |
| Marketing Authorisation Date | 10.07.2020 |
| MA Period of Validity | 10.07.2025 |
| Classification Number | UP/I-530-09/19-01/99 |
| Registration Number | 381-12-01/154-20-06 |
| Prescription | na recept |
| Type of prescription | ponovljivi recept |
| Distribution | u ljekarni |
| Advertising to general public | zabranjeno |
| ATC Code | R03AK07 |
| SmPC | download |
| PL | download |
| Public Assessment Report | download |
| Summary of risk management plan | download |
