Code | 7928C | ||||||||
MA number | 39/0162/18-S | ||||||||
Product Form: | tbl mnd 24x500 mg/1000 IU (strip laminát/Al/papier) | ||||||||
MA Status: | R - Valid Marketing Authorisation | ||||||||
Type of procedure: | Decentralised | ||||||||
Therapeutic Class: | 39 - SOLI A IONTY PRO P.O. A PARENT. APLIKÁCIU | ||||||||
ATC: |
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Shelf life: | 24 | ||||||||
Container: | strip laminate/Al/paper | ||||||||
Route of admin.: | Oral use |
Prescription Status: | Medicinal product subject to medical prescription. |
Legal basis: | Article 10a well-established use application |
MA issued: | 18.05.2018 |
Validity: | 18.05.2023 |
MA renewed: | Renewal application submitted |
Pediatric contraindication: | Yes |
Pediatric warnings: | Yes |
SPC: | SPC_Caltrate D3 500 mg-1000 IU žuvacie tablety_08.2023.pdf |
PIL: | PIL_Caltrate D3 500 mg-1000 IU žuvacie tablety_08.2023.pdf |
Safety feature | Yes |
Data update: | 10.07.2018 |