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PRODUCT DETAIL

Telmisartan Actavis 80 mg tablety

Code 01613
MA number EU/1/10/639/030
Product Form: tbl 250x80 mg (fľa.HDPE)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Actavis Group PTC ehf., Iceland
Therapeutic Class: 58 - HYPOTENSIVA
ATC:
C CARDIOVASCULAR SYSTEM
C09 AGENTS ACTING ON THE RENIN-ANGIOTENSIN SYSTEM
C09C ANGIOTENSIN II ANTAGONISTS, PLAIN
C09CA Angiotensin II antagonists, plain
C09CA07 Telmisartan
Shelf life: 36
Route of admin.: Oral use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 10(1) generic application
MA issued: 30.09.2010
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 21.06.2018
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