VIREAD

This brand name is authorized in Austria, Australia, Brazil, Canada, Cyprus, Germany, Estonia, Spain, Finland, France, Hong Kong, Ireland, Israel, Japan, Lithuania, Mexico, Nigeria, Netherlands, Poland, Romania, Singapore, Turkey, United Kingdom, United States, South Africa

Active ingredients

The drug VIREAD contains one active pharmaceutical ingredient (API):

1 Tenofovir disoproxil
UNII OTT9J7900I - TENOFOVIR DISOPROXIL FUMARATE

Tenofovir disoproxil is absorbed and converted to the active substance tenofovir, which is a nucleoside monophosphate analogue. Tenofovir is then converted to the active metabolite, tenofovir diphosphate, an obligate chain terminator, by constitutively expressed cellular enzymes. Tenofovir diphosphate inhibits HIV-1 reverse transcriptase and the HBV polymerase by direct binding competition with the natural deoxyribonucleotide substrate and, after incorporation into DNA, by DNA chain termination.

Read about Tenofovir disoproxil

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
VIREAD Film-coated tablet European Medicines Agency (EU) MPI, EU: SmPC

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC code Group title Classification
J05AF07 Tenofovir disoproxil J Antiinfectives for systemic use → J05 Antivirals for systemic use → J05A Direct acting antivirals → J05AF Nucleoside and nucleotide reverse transcriptase inhibitors
Discover more medicines within J05AF07

Authorization and marketing

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): 10310P, 11992E
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 546820020000517
Country: CA Health Products and Food Branch Identifier(s): 02247128
Country: DE Bundesinstitut für Arzneimittel und Medizinprodukte Identifier(s): 00567592, 02089470, 02847485, 05013208, 05046834, 05373438, 05373444, 05387386, 06432858, 06432864, 07240546, 09927081, 10532962, 10532979, 10557560, 10757448, 10974341, 11095452, 11554368, 11554374, 12506207, 13569138, 13829970, 16008966, 16008972, 16259958, 16259964
Country: EE Ravimiamet Identifier(s): 1196513, 1365184, 1602234, 1602245, 1602627, 1602638, 1602739, 1602740, 1602841
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 01200001, 101200003, 101200004, 101200006, 101200008
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 009679, 067642, 175826, 451326, 477212
Country: FR Base de données publique des médicaments Identifier(s): 60493359, 64593008, 67279692, 68718936, 69841906
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 220163, 220166, 220170, 220177, 33863
Country: HK Department of Health Drug Office Identifier(s): 56075, 57750
Country: IE Health Products Regulatory Authority Identifier(s): 88408
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 4727
Country: JP 医薬品医療機器総合機構 Identifier(s): 6250024F1021
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1031183, 1064334, 1068567, 1068568, 1068569, 1068570, 1068571, 1068572, 1068573
Country: MX Comisión Federal para la Protección contra Riesgos Sanitarios Identifier(s): 490M2004
Country: NG Registered Drug Product Database Identifier(s): 04-9027
Country: NL Z-Index G-Standaard, PRK Identifier(s): 146595, 146609, 146617, 146625, 146633
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100127594, 100313836, 100313859, 100313871, 100313888
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W51800001, W51800002
Country: SG Health Sciences Authority Identifier(s): 13938P
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8698760090014
Country: US FDA, National Drug Code Identifier(s): 50090-0754, 61958-0401, 61958-0403, 61958-0404, 61958-0405, 61958-0406
Country: ZA Health Products Regulatory Authority Identifier(s): A40/20.2.8/0681

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