This brand name is authorized in Austria, Estonia, Spain, France, Hong Kong, Croatia, Ireland, Japan, Lithuania, Poland, Romania, Turkey, United Kingdom, South Africa
The drug DELTYBA contains one active pharmaceutical ingredient (API):
1
Delamanid
UNII 8OOT6M1PC7 - DELAMANID
|
The pharmacological mode of action of delamanid involves inhibition of the synthesis of the mycobacterial cell wall components, methoxy-mycolic and keto-mycolic acid. The identified metabolites of delamanid do not show anti-mycobacterial activity. |
Below package inserts are available for further reading:
Title | Information Source | Document Type | |
---|---|---|---|
DELTYBA Film-coated tablet | European Medicines Agency (EU) | MPI, EU: SmPC | |
DELTYBA Dispersible tablet | European Medicines Agency (EU) | MPI, EU: SmPC |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC code | Group title | Classification |
---|---|---|
J04AK06 | J Antiinfectives for systemic use → J04 Antimycobacterials → J04A Drugs for treatment of tuberculosis → J04AK Other drugs for treatment of tuberculosis | |
This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
---|---|---|
Country: EE | Ravimiamet | Identifier(s): 1646906, 1646917, 1646928, 1683424, 1862524 |
Country: ES | Centro de información online de medicamentos de la AEMPS | Identifier(s): 113875004 |
Country: FR | Base de données publique des médicaments | Identifier(s): 64639797 |
Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 286220 |
Country: HK | Department of Health Drug Office | Identifier(s): 64412 |
Country: JP | 医薬品医療機器総合機構 | Identifier(s): 6222006F1029 |
Country: LT | Valstybinė vaistų kontrolės tarnyba | Identifier(s): 1075162, 1093371 |
Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100323243 |
Country: RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | Identifier(s): W63026001 |
Country: TR | İlaç ve Tıbbi Cihaz Kurumu | Identifier(s): 8680683090011 |
Country: ZA | Health Products Regulatory Authority | Identifier(s): 52/20.2.3/0460 |
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