Code | 89031 | ||||||||
MA number | 39/0248/10-S | ||||||||
Product Form: | tbl mnd 60x500 mg/800 IU (obal HDPE) | ||||||||
MA Status: | D - Marketing Authorisation valid for an unlimited period | ||||||||
Type of procedure: | Decentralised | ||||||||
MAH, country: | Viatris Healthcare Limited, Ireland | ||||||||
Therapeutic Class: | 39 - SOLI A IONTY PRO P.O. A PARENT. APLIKÁCIU | ||||||||
ATC: |
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Shelf life: | 36 | ||||||||
Container: | HDPE tablet container | ||||||||
Route of admin.: | Oral use |
Prescription Status: | Medicinal product subject to medical prescription. |
Legal basis: | Article 10a well-established use application |
MA issued: | 26.04.2010 |
SPC: | SPC_Kombi-Kalz 500 mg_800 IU žuvacie tablety_11_2022.pdf |
PIL: | PIL_Kombi-Kalz 500 mg_800 IU žuvacie tablety_02_2023.pdf |
Safety feature | Yes |
Data update: | 01.04.2019 |