Fordiab 50 mg/1000 mg filmom obložene tablete
| Name | Fordiab 50 mg/1000 mg filmom obložene tablete |
|---|---|
| Marketing Authorisation Number | HR-H-437058084 |
| Active Substance | sitagliptinklorid hidrat metforminklorid |
| Composition | Jedna tableta sadrži sitagliptinklorid hidrat u količini od 50 mg sitagliptina i 1000 mg metforminklorida |
| Pharmaceutical Form | Filmom obložena tableta |
| Manufacturer | Laboratorios Liconsa S.A., Azuqueca de Henares, Guadalajara, Španjolska STADA Arzneimittel AG, Bad Vilbel, Njemačka |
| Marketing Authorisation Holder | Stada d.o.o., Hercegovačka 14, Zagreb, Hrvatska |
| Marketing Authorisation Date | 27.10.2021 |
| MA Period of Validity | 27.10.2026 |
| Classification Number | UP/I-530-09/19-01/215 |
| Registration Number | 381-12-01/38-21-04 |
| Prescription | na recept |
| Type of prescription | ponovljivi recept |
| Distribution | u ljekarni |
| Advertising to general public | zabranjeno |
| ATC Code | A10BD07 |
| Medicinal product marketed in the Croatia | Da |
| SmPC | download |
| PL | download |
| Public Assessment Report | download |
| Summary of risk management plan | download |
