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PRODUCT DETAIL

Caltrate 600 mg/400 IU D3 filmom obalená tableta

Code 2935B
MA number 39/0359/09-S
Product Form: tbl flm 20x600 mg/400 IU (fľ.PE)
MA Status: D - Marketing Authorisation valid for an unlimited period
Type of procedure: Mutual recognition procedure
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
A12AX01 Calcium carbonate and colecalciferol
Shelf life: 24
Container: bottle PE
Route of admin.: Oral use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 10a well-established use application
MA issued: 14.08.2009
Pediatric warnings: Yes
SPC: SPC_Caltrate 600 mg-400 IU D3 filmom obalená tableta_08.2023.pdf  
PIL: PIL_Caltrate 600 mg-400 IU D3 filmom obalená tableta_08.2023.pdf  
Safety feature Yes
Data update: 01.07.2019
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