ACTELSAR HCT

This brand name is authorized in Austria, Croatia, Estonia, Ireland, Lithuania, Netherlands, Poland, Romania.

Active ingredients

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

1	Telmisartan 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 more about Telmisartan
2	Hydrochlorothiazide UNII 0J48LPH2TH - HYDROCHLOROTHIAZIDE
	Hydrochlorothiazide is a diuretic with antihypertensive properties. It acts by inhibiting the renal tubular re-absorption of sodium and chloride ions, which are excreted with an accompanying volume of water. Potassium excretion is also promoted.
	Read more about Hydrochlorothiazide

Medicine classification

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

ATC Group		Classification
C09DA07	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	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	18132, 18765, 18943
LT	Valstybinė vaistų kontrolės tarnyba	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	67261, 67954
PL	Rejestru Produktów Leczniczych	100075590, 100296919, 100301862
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	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