This brand name is authorized in Austria, Brazil, Germany, Japan
The drug NERISONA contains one active pharmaceutical ingredient (API):
1
Diflucortolone
UNII 1A63Z067C8 - DIFLUCORTOLONE VALERATE
|
Diflucortolone is a topically acting fluoridated corticosteroid which suppresses inflammation in inflammatory and allergic skin conditions and alleviates the subjective complaints such as itching, burning and pain. |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC code | Group title | Classification |
---|---|---|
D07AC06 | Diflucortolone | D Dermatologicals → D07 Corticosteroids, dermatological preparations → D07A Corticosteroids, plain → D07AC Corticosteroids, potent (group III) |
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): 538912050015513, 538912050015613 |
Country: DE | Bundesinstitut für Arzneimittel und Medizinprodukte | Identifier(s): 01692661, 01692721, 04963505, 04963511, 08595352, 08595369, 08595381, 08595398, 17875369 |
Country: JP | 医薬品医療機器総合機構 | Identifier(s): 2646700M1163, 2646700N1150, 2646700N1169, 2646700Q1050 |
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