This brand name is authorized in Austria, Australia, Brazil, Canada, Cyprus, Ecuador, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Israel, Japan, Lithuania, Mexico, Netherlands, New Zealand, Poland, Romania, Singapore, Turkey, United Kingdom, United States, South Africa
The drug INTELENCE contains one active pharmaceutical ingredient (API):
1
Etravirine
UNII 0C50HW4FO1 - ETRAVIRINE
|
Etravirine is an non-nucleoside reverse transcriptase inhibitors (NNRTI) of human immunodeficiency virus type 1 (HIV-1). Etravirine binds directly to reverse transcriptase (RT) and blocks the RNA-dependent and DNA-dependent DNA polymerase activities by causing a disruption of the enzyme’s catalytic site. |
Below package inserts are available for further reading:
Title | Information Source | Document Type | |
---|---|---|---|
INTELENCE 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 |
---|---|---|
J05AG04 | Etravirine | J Antiinfectives for systemic use → J05 Antivirals for systemic use → J05A Direct acting antivirals → J05AG Non-nucleoside reverse transcriptase inhibitors |
This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
---|---|---|
Country: AU | Pharmaceutical Benefits Scheme | Identifier(s): 10301E |
Country: BR | Câmara de Regulação do Mercado de Medicamentos | Identifier(s): 514507601116211, 514514070026903 |
Country: CA | Health Products and Food Branch | Identifier(s): 02306778, 02375931, 02396750 |
Country: EC | Agencia Nacional de Regulación, Control y Vigilancia Sanitaria | Identifier(s): 1951-MEE-0316, 29623-02-11 |
Country: EE | Ravimiamet | Identifier(s): 1381643, 1552788, 1619254 |
Country: ES | Centro de información online de medicamentos de la AEMPS | Identifier(s): 08468002 |
Country: FI | Lääkealan turvallisuus- ja kehittämiskeskus | Identifier(s): 073027 |
Country: FR | Base de données publique des médicaments | Identifier(s): 63514730, 64044237, 66595716 |
Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 142054, 198567 |
Country: HK | Department of Health Drug Office | Identifier(s): 61470 |
Country: IL | מִשְׂרַד הַבְּרִיאוּת | Identifier(s): 6394, 7256 |
Country: JP | 医薬品医療機器総合機構 | Identifier(s): 6250033F1020 |
Country: LT | Valstybinė vaistų kontrolės tarnyba | Identifier(s): 1033738, 1064023, 1070790 |
Country: MX | Comisión Federal para la Protección contra Riesgos Sanitarios | Identifier(s): 347M2008 |
Country: NL | Z-Index G-Standaard, PRK | Identifier(s): 100463, 119709, 88315 |
Country: NZ | Medicines and Medical Devices Safety Authority | Identifier(s): 13404, 14722 |
Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100198482, 100261329, 100302175 |
Country: RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | Identifier(s): W53549001, W61897001, W61898001 |
Country: SG | Health Sciences Authority | Identifier(s): 13597P, 14535P |
Country: TR | İlaç ve Tıbbi Cihaz Kurumu | Identifier(s): 8699593015298 |
Country: US | FDA, National Drug Code | Identifier(s): 59676-570, 59676-571, 59676-572 |
Country: ZA | Health Products Regulatory Authority | Identifier(s): 43/20.2.8/0780, 48/20.2.8/1301 |
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