Ampril HD 5 mg/25 mg tablete
Name | Ampril HD 5 mg/25 mg tablete |
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Marketing Authorisation Number | HR-H-638598704 |
Active Substance | ramipril hidroklorotiazid |
Composition | svaka tableta sadrži 5 mg ramiprila i 25 mg hidroklorotiazida |
Pharmaceutical Form | tableta |
Manufacturer | Krka d.d., Novo mesto, Novo Mesto, Slovenija |
Marketing Authorisation Holder | Krka - farma d.o.o., Radnička cesta 48, Zagreb, Hrvatska |
Marketing Authorisation Date | 31.01.2018 |
MA Period of Validity | unlimited |
Classification Number | UP/I-530-09/17-02/32 |
Registration Number | 381-12-01/30-18-03 |
Prescription | Medicinal product subject to medical prescription |
Type of prescription | ponovljivi recept |
Distribution | Supply through pharmacies (community) |
Advertising to general public | not allowed |
ATC Code | C09BA05 |
Marketing status | stavljeno u promet |
Shortage status | nema nestašice |
SmPC | download |
PL | download |
Packaging
Direct Healthcare Professional Communication
Name | Date | Download |
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Pismo zdravstvenim radnicima o riziku od nemelanomskog raka kože povezanog s primjenom hidroklorotiazida | 17.10.2018 | Alkaloid, Belupo, Berlin-Chemie Menarini, Boehringer Ingelheim International, Farmal, Genericon, Pharma, Jadran Galenski laboratorij, Krka - farma, Merck, Merck Sharp & Dohme, Novartis, PharmaSwiss, Pliva, Sandoz, sanofi-aventis i Stada |