This brand name is authorized in Australia, New Zealand.
The drug MICOLETTE contains a combination of these active pharmaceutical ingredients (APIs):
1
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UNII
B22547B95K - TRISODIUM CITRATE DIHYDRATE
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Potassium citrate is indicated for the management of renal tubular acidosis with calcium stones, hypocitraturic calcium oxalate nephrolithiasis of any etiology, uric acid lithiasis with or without calcium stones. When potassium citrate is given orally, the metabolism of absorbed citrate produces an alkaline load. The induced alkaline load in turn increases urinary pH and raises urinary citrate by augmenting citrate clearance without measurably altering ultrafilterable serum citrate. Thus, potassium citrate therapy appears to increase urinary citrate principally by modifying the renal handling of citrate, rather than by increasing the filtered load of citrate. |
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2
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UNII
D0Y70F2B9J - SODIUM LAURYL SULFOACETATE
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3
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UNII
506T60A25R - SORBITOL
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This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| A06AG20 | Combinations | A Alimentary tract and metabolism → A06 Laxatives → A06A Laxatives → A06AG Enemas |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| AU | Pharmaceutical Benefits Scheme | 2091C, 3274H, 4462W, 5331N |
| NZ | Medicines and Medical Devices Safety Authority | 11824 |
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