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

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:

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