Neodol 200 mg oralna suspenzija u vrećici
Name | Neodol 200 mg oralna suspenzija u vrećici |
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Former Name | Rapidol S 200 mg oralna suspenzija u vrećici |
Marketing Authorisation Number | HR-H-288791324 |
Active Substance | ibuprofen |
Composition | svaka jednodozna vrećica sadrži 200 mg ibuprofena u 10 ml oralne suspenzije jedan mililitar oralne suspenzije sadrži 20 mg ibuprofena |
Pharmaceutical Form | oralna suspenzija u vrećici |
Manufacturer | Farmalider S.A., Alcobendas - Madrid, Španjolska Edefarm S.L., Villamarchante, Valencia, Španjolska Zinereo Pharma, S.L., O Porrino, Pontevedra, Španjolska |
Marketing Authorisation Holder | Jadran Galenski laboratorij d.d., Svilno 20, Rijeka, Hrvatska |
Marketing Authorisation Date | 10.10.2022 |
MA Period of Validity | unlimited |
Classification Number | UP/I-530-09/21-02/208 |
Registration Number | 381-12-01/154-22-04 |
Prescription | Medicinal product not subject to medical prescription |
Distribution | Supply through pharmacies (community) |
Advertising to general public | allowed |
ATC Code | M01AE01 |
Marketing status | stavljeno u promet |
Shortage status | nema nestašice |
SmPC | download |
PL | download |
Public Assessment Report | download |