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SOFOSBUVIR & VELPATASVIR

All products: Limited Use (codes 488)

Other products in the same Health Canada class (J05A, J05AP) — coverage varies; not interchangeable

  • Glecaprevir + pibrentasvir (Maviret): limited Use 550, 551, 552
  • Ledipasvir + sofosbuvir (Harvoni): limited Use 482, 483, 484
  • Sofosbuvir (Sovaldi): limited Use 485, 487
  • Abacavir + lamivudine + zidovudine (Trizivir): general benefit
  • Abacavir (Ziagen): general benefit
  • Abacavir + lamivudine (Kivexa): general benefit

47 more in the class list below

Epclusa · DIN 02456370 · 400mg & 100mg · tablet

Limited Use — Reason for Use code 488 requiredMarketed · checked 2026-09-02
StatusLimited Use — Reason for Use code 488 required
Write on scriptLU code 488 (patient must meet the criteria below)
Patient paysPatient pays: program not supplied; amount cannot be determined.
Private plan unknown: ask. If yes, check its coverage and payer coordination; if no, see the public routes below.
Ontario Limited Use criteria — code 488
Reason for Use code 488 For treatment-naive or treatment-experienced (1) adult patients with chronic hepatitis C (CHC) infection who meet all the following criteria: (i) Treatment is prescribed by a hepatologist, gastroenterologist, infectious disease specialist or other prescriber experienced in treating chronic hepatitis C; AND (ii) Laboratory confirmed hepatitis C genotype 1, 2, 3, 4, 5, 6 or mixed genotypes; AND (iii) Established chronicity of HCV infection either by two laboratory confirmed quantitative HCV RNA values taken at least 6 months apart; OR One recent laboratory confirmed quantitative HCV RNA within the past 6 months and clinical features establishing a duration of HCV infection longer than 6 months (e.g. presence of fibrosis, presence of non-liver manifestations of HCV, prolonged ALT elevation greater than 6 months without another cause, HCV antibody positivity greater than 6 months), or risk factors for HCV acquisition greater than 6 months (e.g. injection drug use). Treatment regimens for Epclusa (sofosbuvir-velpatasvir): I. Treatment-naive or treatment-experienced (1) non-cirrhotic or compensated cirrhosis (2) Approved duration: 12 weeks II. Treatment-naive or treatment-experienced patients with decompensated cirrhosis (2) Approved regimen: 12 weeks in combination with ribavirin (Ibavyr) Retreatment is not funded. Retreatment for failure or re-infection in patients who have received an adequate prior course of direct-acting antiviral will be considered on a case-by-case basis through the Exceptional Access Program. Coverage limit: LU Authorization Period: 12 Weeks. Coverage limit: 1. Treatment-experienced are those who failed prior therapy with an interferon-based regimen, including regimens containing an HCV protease inhibitor. 2. Compensated cirrhosis (Child-Turcotte-Pugh A [i.e. Scores 5 to 6]) and decompensated cirrhosis (Child-Turcotte-Pugh B or C [i.e. Score 7 or above]) may be considered. 3. Health care professionals are advised to refer to the product monograph and prescribing guidelines for appropriate use of the drug product, including use in special populations.
No interchangeable product listed in the Ontario extract
Epclusa · DIN 02456370 Manufacturer: Gilead Sciences Canada, Inc.; listing date 2017-02-28 Health Canada: Marketed since 2016-08-02 · brand EPCLUSA · ATC J05AP55 SOFOSBUVIR AND VELPATASVIR, J05AP55 SOFOSBUVIR AND VELPATASVIR · form Tablet · route Oral · ingredients SOFOSBUVIR 400 MG, VELPATASVIR 100 MG · company Gilead sciences canada inc · schedule Prescription
Check this DIN again · Health Canada product record

Epclusa: Formulary list price $714.2857/unit (unit not stated in source; not the patient's cost)

Ministry pays: $714.2857 per source unit.

Source explanation: The formulary price is what ODB pays; the cash price at the counter is set by the pharmacy.

Formulary data: Ontario extract of Aug 26, 2026 · Health Canada DPD extract of Sep 2, 2026 (Open Government Licence – Canada) · https://health-products.canada.ca/dpd-bdpp/info?lang=eng&code=94324 · Verify on the e-Formulary ↗ (DIN 02456370)

Source record
DIN 02456370: Epclusa Raw flags: sec12=Y, sec3=Y Item: 081800382; group id 110; item number 0192; lccId 00278; manufacturer id GIL Source form: Tab; strength: 400mg & 100mg Recorded listing: Limited Use: paid only with a Reason for Use code and the criteria below Source prices (unrounded): $714.2857; ministry $714.2857 Source: ODB odb-formulary-ed43-extract-2026-08-26.xml extract_date=2026-08-26 DIN=02456370 Health Canada DPD extract of Sep 2, 2026 (Open Government Licence – Canada) · https://health-products.canada.ca/dpd-bdpp/info?lang=eng&code=94324
Shortage status: no shortage or discontinuation reported (checked 2026-09-13T08:10:21.292534+00:00); reports as of 2026-09-13T08:10:21.292534+00:00 (Health Product Shortages Canada) Source: https://healthproductshortages.ca/search?term=02456370
Shortage record checked 2026-09-13T08:10:21.292534+00:00

SOFOSBUVIR & VELPATASVIR & VOXILAPREVIR

All products: Limited Use (codes 524)

Other products in the same Health Canada class (J05A, J05AP) — coverage varies; not interchangeable

  • Glecaprevir + pibrentasvir (Maviret): limited Use 550, 551, 552
  • Ledipasvir + sofosbuvir (Harvoni): limited Use 482, 483, 484
  • Sofosbuvir (Sovaldi): limited Use 485, 487
  • Abacavir + lamivudine + zidovudine (Trizivir): general benefit
  • Abacavir (Ziagen): general benefit
  • Abacavir + lamivudine (Kivexa): general benefit

47 more in the class list below

Vosevi · DIN 02467542 · 400mg & 100mg & 100mg · tablet

Limited Use — Reason for Use code 524 requiredMarketed · checked 2026-09-02
StatusLimited Use — Reason for Use code 524 required
Write on scriptLU code 524 (patient must meet the criteria below)
Patient paysPatient pays: program not supplied; amount cannot be determined.
Private plan unknown: ask. If yes, check its coverage and payer coordination; if no, see the public routes below.
Ontario Limited Use criteria — code 524
Reason for Use code 524 For treatment-experienced (1) adult patients with chronic hepatitis C (CHC) infection who meet all the following criteria: (i) Treatment is prescribed by a hepatologist, gastroenterologist, infectious disease specialist or other prescriber experienced in treating chronic hepatitis C; AND (ii) Laboratory confirmed hepatitis C genotype 1, 2, 3, 4, 5, 6 or mixed genotypes; AND (iii) Established chronicity of HCV infection either by two laboratory confirmed quantitative HCV RNA values taken at least 6 months apart; OR One recent laboratory confirmed quantitative HCV RNA within the past 6 months and clinical features establishing a duration of HCV infection longer than 6 months (e.g. presence of fibrosis, presence of non-liver manifestations of HCV, prolonged ALT elevation greater than 6 months without another cause, HCV antibody positivity greater than 6 months), or risk factors for HCV acquisition greater than 6 months (e.g. injection drug use). Treatment regimen for Vosevi (sofosbuvir-velpatasvir-voxilaprevir): Treatment-experienced, non-cirrhotic or compensated cirrhosis (2) Approved duration: 12 weeks Retreatment is not funded. Retreatment for failure or re-infection in patients who have received an adequate prior course of Vosevi will be considered on a case-by-case basis through the Exceptional Access Program. Coverage limit: LU Authorization Period: 12 Weeks. Coverage limit: 1. Treatment-experienced are those who failed prior therapy with a HCV regimen containing: i. NS5A inhibitor* for genotype 1, 2, 3, 4, 5, or 6; OR ii. Sofosbuvir (Sovaldi) without an NS5A inhibitor for genotype 1, 2, 3, or 4 *NS5A inhibitors include: daclatasvir (Daklinza), elbasvir (as part of Zepatier), ledipasvir (as part of Harvoni), ombitasvir (as part of Holkira Pak), velpatasvir (as part of Epclusa), pibrentasvir (as part of Maviret) 2. Compensated cirrhosis (Child-Turcotte-Pugh A [i.e. Scores 5 to 6]) may be considered. 3. Health care professionals are advised to refer to the product monograph and prescribing guidelines for appropriate use of the drug product, including use in special populations.
No interchangeable product listed in the Ontario extract
Vosevi · DIN 02467542 Manufacturer: Gilead Sciences Canada, Inc.; listing date 2018-02-28 Health Canada: Marketed since 2017-09-18 · brand VOSEVI · ATC J05AP56 SOFOSBUVIR, VELPATASVIR AND VOXILAPREVIR · form Tablet · route Oral · ingredients VELPATASVIR 100 MG, SOFOSBUVIR 400 MG, VOXILAPREVIR 100 MG · company Gilead sciences canada inc · schedule Prescription
Check this DIN again · Health Canada product record

Vosevi: Formulary list price $714.2857/unit (unit not stated in source; not the patient's cost)

Ministry pays: $714.2857 per source unit.

Source explanation: The formulary price is what ODB pays; the cash price at the counter is set by the pharmacy.

Formulary data: Ontario extract of Aug 26, 2026 · Health Canada DPD extract of Sep 2, 2026 (Open Government Licence – Canada) · https://health-products.canada.ca/dpd-bdpp/info?lang=eng&code=95590 · Verify on the e-Formulary ↗ (DIN 02467542)

Source record
DIN 02467542: Vosevi Raw flags: sec12=Y, sec3=Y Item: 081800389; group id 111; item number 0193; lccId 00298; manufacturer id GIL Source form: Tab; strength: 400mg & 100mg & 100mg Recorded listing: Limited Use: paid only with a Reason for Use code and the criteria below Source prices (unrounded): $714.2857; ministry $714.2857 Source: ODB odb-formulary-ed43-extract-2026-08-26.xml extract_date=2026-08-26 DIN=02467542 Health Canada DPD extract of Sep 2, 2026 (Open Government Licence – Canada) · https://health-products.canada.ca/dpd-bdpp/info?lang=eng&code=95590
Shortage status: no shortage or discontinuation reported (checked 2026-09-13T08:10:21.292534+00:00); reports as of 2026-09-13T08:10:21.292534+00:00 (Health Product Shortages Canada) Source: https://healthproductshortages.ca/search?term=02467542
Shortage record checked 2026-09-13T08:10:21.292534+00:00
Other drugs in the same formulary class (08:18 Antivirals) and how they are covered

Matched class: 08:18 Antivirals

Drug-class inventory only. Lists recorded Ontario formulary products, not every Canadian medication; does not recommend treatment. Covered without a code on the Ontario formulary: ABACAVIR & LAMIVUDINE & ZIDOVUDINE, ABACAVIR SULFATE, ABACAVIR SULFATE & LAMIVUDINE, BICTEGRAVIR SODIUM/EMTRICITABINE/TENOFOVIR ALAFENAMIDE HEMIFUMARATE, CABOTEGRAVIR, CABOTEGRAVIR & RILPIVIRINE, COBICISTAT & ELVITEGRAVIR & EMTRICITABINE & TENOFOVIR DISOPROXIL FUMARATE, DARUNAVIR & COBICISTAT, DARUNAVIR & COBICISTAT & EMTRICITABINE & TENOFOVIR ALAFENAMIDE, DELAVIRDINE MESYLATE, DOLUTEGRAVIR, DOLUTEGRAVIR & ABACAVIR & LAMIVUDINE, DOLUTEGRAVIR & RILPIVIRINE, DOLUTEGRAVIR SODIUM/LAMIVUDINE, DORAVIRINE, DORAVIRINE/LAMIVUDINE/TENOFOVIR DISOPROXIL FUMARATE, EFAVIRENZ/TENOFOVIR DISOPROXIL FUMARATE/EMTRICITABINE, ELVITEGRAVIR & COBICISTAT & EMTRICITABINE & TENOFOVIR ALAFENAMIDE, EMTRICITABINE & RILPIVIRINE HCL & TENOFOVIR ALAFENAMIDE HEMIFUMARATE, EMTRICITABINE & RILPIVIRINE HCL & TENOFOVIR DISOPROXIL, EMTRICITABINE & TENOFOVIR DISOPROXIL FUMARATE, ETRAVIRINE, FOSAMPRENAVIR CALCIUM, GANCICLOVIR SODIUM, LAMIVUDINE & ZIDOVUDINE, LOPINAVIR & RITONAVIR, MARAVIROC, NELFINAVIR MESYLATE, RALTEGRAVIR POTASSIUM, RILPIVIRINE HYDROCHLORIDE, RITONAVIR Some products covered without a code (check the product listing): ACYCLOVIR, ATAZANAVIR SULFATE, DARUNAVIR, EFAVIRENZ, LAMIVUDINE, NEVIRAPINE, VALACYCLOVIR 08:18 Antivirals

GLECAPREVIR & PIBRENTASVIR

· 1 products · Limited Use, codes 550, 551, 552 · strengths: 100mg & 40mg · Tab

LEDIPASVIR & SOFOSBUVIR

· 1 products · Limited Use, codes 482, 483, 484 · strengths: 90mg & 400mg · Tab

SOFOSBUVIR

· 1 products · Limited Use, codes 485, 487 · strengths: 400mg · Tab

ABACAVIR & LAMIVUDINE & ZIDOVUDINE

· 2 products · General benefit · strengths: 300mg & 150mg & 300mg · Tab

ABACAVIR SULFATE

· 4 products · General benefit · strengths: 20mg/mL, 300mg · O/L, Tab

ABACAVIR SULFATE & LAMIVUDINE

· 7 products · General benefit · strengths: 600mg & 300mg · Tab

ACYCLOVIR

· 15 products · Listed, not a benefit (2), General benefit (13) · strengths: 200mg, 400mg, 800mg · Tab

ATAZANAVIR SULFATE

· 12 products · General benefit (8), Off-Formulary Interchangeable, not an ODB benefit (4) · strengths: 150mg, 200mg, 300mg · Cap

BICTEGRAVIR SODIUM/EMTRICITABINE/TENOFOVIR ALAFENAMIDE HEMIFUMARATE

· 1 products · General benefit · strengths: 50mg & 200mg & 25mg · Tab

CABOTEGRAVIR

· 3 products · General benefit · strengths: 200mg/mL, 30mg · Inj Sol-ER Susp 3mL Vial Kit Pk, Tab

CABOTEGRAVIR & RILPIVIRINE

· 2 products · General benefit · strengths: 200mg/mL & 300mg/mL · Inj Sol-2mL Kit, Inj Sol-3mL Kit

COBICISTAT & ELVITEGRAVIR & EMTRICITABINE & TENOFOVIR DISOPROXIL FUMARATE

· 1 products · General benefit · strengths: 150mg & 150mg & 200mg & 300mg · Tab Source: formulary-ed43-front-matter.txt Part V; ODB odb-formulary-ed43-extract-2026-08-26.xml extract_date=2026-08-26; class 08:18 and 41 more
Full class listing Related classes: 08:08 Anthelmintics, 08:12 Antibiotics, 08:14 Antifungals, 08:16 Antitubercular Agents, 08:20 Plasmodicides (Antimalarials), 08:24 Sulfonamides, 08:30 Antiprotozoals, 08:32 Trichomonacides, 08:36 Urinary Anti-Infectives, 08:40 Miscellaneous Anti-Infectives Same formulary class, not same indication: class membership alone does not establish equivalent uses.
Other drugs whose Health Canada label lists a similar indication: hepatitis c virus
From Health Canada product monographs; label wording only, not a treatment recommendation. Matching is lexical and uses one held product label per generic; formulations and qualifying criteria may differ. No displayed matched alternative is a general benefit. GLECAPREVIR & PIBRENTASVIR · Limited Use, codes 550, 551, 552 Indications MAVIRET (glecaprevir/pibrentasvir) is indicated for the treatment of acute and chronic hepatitis C virus (HCV) infection in adults and pediatric patients 3 years of age and older and weighing ≥ 12 kg (see 4. PM: https://pdf.hres.ca/dpd_pm/00082890.PDF; date 2025-12-18; DIN 02467550; fetched 2026-09-10 Product monograph LEDIPASVIR & SOFOSBUVIR · Limited Use, codes 482, 483, 484 1 INDICATIONS HARVONI (ledipasvir/sofosbuvir) is indicated for the treatment of chronic hepatitis C virus (CHC) infection in adults (≥ 18 years of age). PM: https://pdf.hres.ca/dpd_pm/00061949.PDF; date October 15, 2014; DIN 02432226; fetched 2026-09-10 Product monograph Coverage source: ON formulary extract 2026-08-26
What the Health Canada label says it is for
1 INDICATIONS EPCLUSA (sofosbuvir/velpatasvir) is indicated for the treatment of chronic hepatitis C virus (HCV) infection:  in adults and pediatric patients ≥ 12 years of age and weighing ≥ 30 kg without cirrhosis or with compensated cirrhosis  in combination with ribavirin in adults with decompensated cirrhosis. Patients Co-infected with Human Immunodeficiency Virus (HIV-1) Safety and efficacy have been established in HCV-infected adult patients, with or without cirrhosis, who are co-infected with HIV-1 (see 4 DOSAGE AND ADMINISTRATION and 14 CLINICAL TRIALS). Safety and efficacy have not been studied in pediatric patients co-infected with HIV-1. The treatment of pediatric patients ≥ 12 years of age and weighing ≥ 30 kg and co -infected with HIV-1 is based on extrapolation of relevant clinical data (see 10 CLINICAL PHARMACOLOGY and 14 CLINICAL TRIALS). 1.1 Pediatrics (<18 years of age) The safety and efficacy of EPCLUSA in pediatric patients ≥ 12 years of age receiving EPCLUSA once daily have been established (see 8 ADVERSE REACTIONS and 14 CLINICAL TRIALS). Exposures to EPCLUSA in pediatric patients ≥ 12 to <18 years of age and weigh… https://pdf.hres.ca/dpd_pm/00066982.PDF PM date: August 8, 2022 Source product: EPCLUSA; DIN 02456370; fetched 2026-09-10 Product monograph posted by Health Canada; excerpt for lookup only.
What the Health Canada label says it is for
1 INDICATIONS VOSEVI (sofosbuvir/velpatasvir/voxilaprevir) is indicated for the treatment of chronic hepatitis C virus (HCV) infection in adult patients, without cirrhosis or with compensated cirrhosis, who have:  genotype 1, 2, 3, 4, 5, or 6 infection and have previously been treated with an HCV regimen containing an NS5A inhibitor;  genotype 1, 2, 3, or 4 infection and have been previously treated with an HCV regimen containing sofosbuvir without an NS5A inhibitor. 1.1 Pediatrics (<18 years of age) Safety and effectiveness in pediatric patients have not been established. Therefore, Health Canada has not authorized an indication for pediatric use in patients less than 18 years of age. 1.2 Geriatrics (≥ 65 years of age) The response rates observed for patients 65 years of age and over were similar to those of younger patients across treatment groups. VOSEVI can be administered in geriatric patients (see 10 CLINICAL PHARMACOLOGY and 14 CLINICAL TRIALS). https://pdf.hres.ca/dpd_pm/00061133.PDF PM date: May 19, 2021 Source product: VOSEVI; DIN 02467542; fetched 2026-09-10 Product monograph posted by Health Canada; excerpt for lookup only.