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PRODUCT DETAIL

Caltrate D3 500 mg/1000 IU žuvacie tablety

Code 7930C
MA number 39/0162/18-S
Product Form: tbl mnd 48x500 mg/1000 IU (strip laminát/Al/papier)
MA Status: D - Marketing Authorisation valid for an unlimited period
Type of procedure: Decentralised
MAH, country: Haleon Czech Republic s.r.o., Czechia
Therapeutic Class: 39 - SOLI A IONTY PRO P.O. A PARENT. APLIKÁCIU
ATC:
A ALIMENTARY TRACT AND METABOLISM
A12 MINERAL SUPPLEMENTS
A12A CALCIUM, PLAIN
A12AX Calcium, combinations with vitamin D and/or other drugs
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
Pediatric contraindication: Yes
Pediatric warnings: Yes
PIL: PIL_Caltrate D3 500 mg_1000 IU žuvacie tablety_06_2024.pdf  
SPC: SPC_Caltrate D3 500 mg_1000 IU žuvacie tablety_06_2024.pdf  
Safety feature Yes
Data update: 18.07.2024
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