Bupensanduo 2 mg/0,5 mg sublingvalne tablete
Name | Bupensanduo 2 mg/0,5 mg sublingvalne tablete |
---|---|
Marketing Authorisation Number | HR-H-735309760 |
Active Substance | buprenorfinklorid naloksonklorid dihidrat |
Composition | svaka sublingvalna tableta sadrži 2 mg buprenorfina (u obliku klorida) i 0,5 mg naloksona (u obliku klorid dihidrata). |
Pharmaceutical Form | sublingvalna tableta |
Packaging [MA Number for Packaging] | 7 tableta u blisteru, u kutiji [HR-H-735309760-01] 28 tableta u blisteru, u kutiji [HR-H-735309760-02] 49 tableta u blisteru, u kutiji [HR-H-735309760-03] 56 tableta u blisteru, u kutiji [HR-H-735309760-04] 7 tableta u blisteru s jediničnom dozom, u kutiji [HR-H-735309760-05] 28 tableta u blisteru s jediničnom dozom, u kutiji [HR-H-735309760-06] 49 tableta u blisteru s jediničnom dozom, u kutiji [HR-H-735309760-07] 56 tableta u blisteru s jediničnom dozom, u kutiji [HR-H-735309760-08] |
Manufacturer | G.L. Pharma GmbH, Lannach, Austrija |
Marketing Authorisation Holder | G.L. Pharma GmbH, Schlossplatz 1, Lannach, Austrija |
Marketing Authorisation Date | 16.05.2018 |
MA Period of Validity | 16.05.2023 |
Classification Number | UP/I-530-09/17-01/29 |
Registration Number | 381-12-01/70-18-08 |
Prescription | na recept |
Type of prescription | poseban recept |
Distribution | u ljekarni |
Advertising to general public | zabranjeno |
ATC Code | N07BC51 |
Medicinal product marketed in the Croatia | Nestašica |
SmPC | download |
PL | download |
Public Assessment Report | download |