This brand name is authorized in Brazil, Singapore, South Africa
The drug PRELONE contains one active pharmaceutical ingredient (API):
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1
Prednisolone
UNII 9PHQ9Y1OLM - PREDNISOLONE
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Prednisolone is a glucocorticoid which has anti-inflammatory activity. Naturally occurring glucocorticoids (hydrocortisone and cortisone), which also have salt-retaining properties, are used as replacement therapy in adrenocortical deficiency states. Their synthetic analogs are primarily used for their potent anti-inflammatory effects in disorders of many organ systems. |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC code | Group title | Classification |
|---|---|---|
| H02AB06 | Prednisolone | H Systemic hormonal preparations, excl. Sex hormones and insulins → H02 Corticosteroids for systemic use → H02A CORTICOSTEROIDS FOR SYSTEMIC USE, PLAIN → H02AB Glucocorticoids |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| Country: BR | Câmara de Regulação do Mercado de Medicamentos | Identifier(s): 500509401130413, 500509402110416, 500509403133411, 500509404113412, 500509405136416, 500509406132414, 500509407112311, 500509408135313 |
| Country: SG | Health Sciences Authority | Identifier(s): 04845P |
| Country: ZA | Health Products Regulatory Authority | Identifier(s): 28/21.5.1/0158 |
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