LEVITRA

20MG TBL FLM 12 I

SÚKL code 0025900
Name of the product LEVITRA
_MA_MEDICATION_DETAIL_INFO_MED_NAME i LEVITRA
Supplement 20MG TBL FLM 12 I
Strenght 20MG
Pharmaceutical form Film-coated tablet
Package 12 I
Route Oral use
Wrap type Blister
Legal status na lékařský předpis
Active substance VARDENAFIL HYDROCHLORIDE (VARDENAFILI HYDROCHLORIDUM)
ATC group G04BE09
ATC group name VARDENAFIL

Marketing authorisation information

Registration Number EU/1/03/248/012
Type of MA centralised without orphans
MA status R - active MA/authorised medicinal product
MA Holder Bayer AG, Leverkusen
MA Holder country NĚMECKO

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