ACTELSAR HCT

This brand name is authorized in the following countries: Austria Estonia Ireland Lithuania Netherlands Poland Romania

Active ingredients

The drug ACTELSAR HCT contains a combination of these active pharmaceutical ingredients (APIs):

UNII U5SYW473RQ - TELMISARTAN

Telmisartan is an orally active and specific angiotensin II receptor (type AT1) antagonist. Telmisartan selectively binds the AT1 receptor. The binding is long-lasting.

Read about Telmisartan
UNII 0J48LPH2TH - HYDROCHLOROTHIAZIDE

Hydrochlorothiazide is a diuretic and an antihypertensive agent. It affects the distal renal tubular mechanism of electrolyte reabsorption and increases excretion of sodium and chloride in approximately equivalent amounts.

Read about Hydrochlorothiazide

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC code
Group title
Classification
Telmisartan and diuretics
C Cardiovascular system → C09 Agents acting on the renin-angiotensin system → C09D Angiotensin II antagonists, combinations → C09DA Angiotensin II antagonists and diuretics
Discover more medicines within C09DA07

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country
Identification scheme
Identifier(s)
EE
Ravimiamet
Identifier(s): 1609859, 1609860, 1609871, 1609882, 1609893, 1609905, 1609916, 1609927, 1609938, 1609949, 1609950, 1609961, 1609972, 1609983, 1609994, 1610008, 1610019, 1610020, 1610031, 1610042, 1610053, 1610064, 1664401, 1664412
IE
Health Products Regulatory Authority
Identifier(s): 18132, 18765, 18943
LT
Valstybinė vaistų kontrolės tarnyba
Identifier(s): 1069703, 1069704, 1069705, 1069706, 1069707, 1069708, 1069709, 1069710, 1069711, 1069712, 1069713, 1069714, 1069715, 1069716, 1069717, 1069718, 1069719, 1069720, 1069721, 1069722, 1069723, 1069724, 1069725, 1069726, 1069727, 1069728, 1069729, 1069730, 1069731, 1069732, 1069733, 1069734, 1069735, 1069736, 1069737, 1069738, 1069739, 1069740, 1069741, 1069742, 1069743, 1074191, 1074192, 1074193, 1074194, 1074195
NL
Z-Index G-Standaard, PRK
Identifier(s): 67261, 67954
PL
Rejestru Produktów Leczniczych
Identifier(s): 100075590, 100296919, 100301862
RO
Agenția Națională a Medicamentului și a Dispozitivelor Medicale
Identifier(s): W59717001, W59717002, W59717003, W59717004, W59717005, W59717006, W59717007, W59717008, W59717009, W59717010, W59717011, W59717012, W59717013, W59718001, W59718002, W59718003, W59718004, W59718005, W59718006, W59718007, W59718008, W59718009, W59718010, W59718011, W59718012, W59718013, W59718014, W59718015, W59719001, W59719002, W59719003, W59719004, W59719005, W59719006, W59719007, W59719008, W59719009, W59719010, W59719011, W59719012, W59719013

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