This brand name is authorized in Nigeria.
The drug CARDIOTAN HCT contains a combination of these active pharmaceutical ingredients (APIs):
1
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UNII
864V2Q084H - AMLODIPINE BESYLATE
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Amlodipine is a calcium ion influx inhibitor of the dihydropyridine group (slow channel blocker or calcium ion antagonist) and inhibits the transmembrane influx of calcium ions into cardiac and vascular smooth muscle. |
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2
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UNII
U5SYW473RQ - TELMISARTAN
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Telmisartan is an orally active and specific angiotensin II receptor (type AT1) antagonist. Telmisartan selectively binds the AT1 receptor. The binding is long-lasting. |
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3
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UNII
0J48LPH2TH - HYDROCHLOROTHIAZIDE
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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. |
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This drug has been approved in Nigeria as follows:
| Identifier | Form | Presentation | Description | Approval |
|---|---|---|---|---|
| A4-100789 | Tablet | Cardiotan HCT Tablet 80/10/12.5 mg TAB 10 mg; 80 mg; 12.5 mg 3 x 10's; 10 x 10's (in Alu-Alu blisters) | Uncoated Tablet. Pink and white colored bilayered, round, biconvex tablet, having break line on one side and plain on other side | 27/03/2024 |
| A4-100790 | Tablet | Cardiotan HCT Tablet 40/5/12.5 mg TAB 5 mg; 40 mg; 12.5 mg 3 x 10's; 10 x 10's (in Alu-Alu blisters) | Uncoated Tablet. Pink and white colored bilayered, round, biconvex tablets, both sides plain | 27/03/2024 |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| C09DX08 | C Cardiovascular system → C09 Agents acting on the renin-angiotensin system → C09D Angiotensin II antagonists, combinations → C09DX Angiotensin II antagonists, other combinations | |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| NG | Registered Drug Product Database | A4-100789, A4-100790 |
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