Velafax 37,5 mg tablete
| Name | Velafax 37,5 mg tablete |
|---|---|
| Marketing Authorisation Number | HR-H-177089893 |
| Active Substance | venlafaksinklorid |
| Composition | jedna tableta sadrži 37,5 mg venlafaksina u obliku venlafaksinklorida |
| Pharmaceutical Form | tableta |
| Manufacturer | Pliva Hrvatska d.o.o., Zagreb, Hrvatska |
| Marketing Authorisation Holder | Pliva Hrvatska d.o.o., Prilaz baruna Filipovića 25, Zagreb, Hrvatska |
| Marketing Authorisation Date | 16.02.2015 |
| MA Period of Validity | unlimited |
| Classification Number | UP/I-530-09/14-02/07 |
| Registration Number | 381-12-01/30-15-07 |
| Prescription | na recept |
| Type of prescription | ponovljivi recept |
| Distribution | u ljekarni |
| Advertising to general public | zabranjeno |
| ATC Code | N06AX16 |
| Medicinal product marketed in the Croatia | Da |
| SmPC | download |
| PL | download |
