US FDA United States — FDA approvals (Drugs@FDA)
| Product | Strength | Form · route | Applicant | Status | First approved |
| JULUCA | EQ 50MG BASE;EQ 25MG BASE | tablet · oral | VIIV HLTHCARE | Prescription | 21 Nov 2017 |
EMA European Union — centrally authorised medicines
Juluca ViiV Healthcare B.V. · Authorised · authorised 16 May 2018 · ATC J05AR
Therapeutic indication (EMA)
Juluca is indicated for the treatment of human immunodeficiency virus type 1 (HIV-1) infection in adults who are virologically-suppressed (HIV-1 RNA <50 copies/mL) on a stable antiretroviral regimen for at least six months with no history of virological failure and no known or suspected resistance to any non-nucleoside reverse transcriptase inhibitor or integrase inhibitor.
Canada Canada — marketed products (Health Canada)
| Brand | DIN | Strength | Form · route | Company |
| JULUCA | 02475774 | 50 MG; 25 MG | TABLET · ORAL | VIIV HEALTHCARE ULC |
Prices — United States and England
| Source | Product as listed | Price | Unit / pack | Date |
| US NADAC | JULUCA 50-25 MG TABLET | $121.86639 | per EA | 23 Sep 2026 |
NADAC: average price US retail pharmacies pay to buy the medicine. NHS Drug Tariff Part VIIIA: basic price reimbursed to pharmacies in England and Wales.
Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.