This brand name is authorized in South Africa
The drug AMILORETIC contains a combination of these active pharmaceutical ingredients (APIs):
1
Amiloride
UNII FZJ37245UC - AMILORIDE HYDROCHLORIDE
|
Amiloride has mild diuretic and anti-hypertensive activity. It acts primarily in the distal tubule and does not require aldosterone for its action. Amiloride is a mild natriuretic which does not initiate a concomitant decrease in potassium levels. |
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. |
Below package inserts are available for further reading:
Title | Information Source | Document Type | |
---|---|---|---|
AMILORETIC Tablet | Health Products Regulatory Authority (ZA) | MPI, Generic |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC code | Group title | Classification |
---|---|---|
C03AX01 | Hydrochlorothiazide, combinations | C Cardiovascular system → C03 Diuretics → C03A Low-ceiling diuretics, thiazides → C03AX Thiazides, combinations with other drugs |
This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
---|---|---|
Country: ZA | Health Products Regulatory Authority | Identifier(s): L/18.1/396, U/18.1/40 |
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