Look up one drug

Ontario coverage, price, criteria word for word, Health Canada status and shortages for one product

Patient plan: look up a medication list

BILASTINE

All products: not a benefit

Other products in the same Health Canada class (R06A, R06AX) — coverage varies; not interchangeable

  • Loratadine (Claritin): not a benefit
  • Rupatadine (Rupall): not a benefit
  • Cetirizine (Reactine): not a benefit

Blexten · DIN 02454130 · 20mg · tablet

Off-Formulary Interchangeable, not an ODB benefitMarketed · checked 2026-09-19
StatusOff-Formulary Interchangeable, not an ODB benefit
Write on scriptnot a benefit; no Exceptional Access criteria on record; see alternatives
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.
Brand vs generic price
Lowest DBP recovery rule under medically necessary no-substitution claims: 6.2 Medically Necessary "No Substitution" Claims The Side Effect Reporting Form will not have to be renewed. However, the pharmacy must maintain a copy of the prescription that contains a direction that there be no substitution and the required Health Canada Side Effect Reporting Form (completed and signed by the prescriber). The prescriber must write “No Substitution” or “No Sub” on renewal or subsequent new written prescriptions, and indicate “No Substitution” on subsequent new oral prescriptions. The dispenser will be reimbursed the DBP plus a mark-up and the lesser of the posted usual and customary fee or the ODB dispensing fee minus the applicable ODB co-payment amount. Where a completed Side Effect Reporting Form is not available at the pharmacy during an inspection, the difference between the cost of the higher-cost product and the lowest DBP listed for the interchangeable category will be recovered. (ontario.ca, Revision #17; 2026-08-03 ↗) 6.2 Medically Necessary "No Substitution" Claims The Ministry will provide reimbursement of a higher-cost interchangeable product in medically necessary circumstances where a patient has experienced a significant adverse reaction with two (2) lower-cost interchangeable drug products, where available. When a prescriber identifies a patient for which it is medically necessary that a higher cost interchangeable product be provided, the prescriber must: • Complete, sign and forward to the pharmacist a copy of the Health Canada side effect reporting form for each lower-cost interchangeable drug product trialed (Side Effect Reporting Form[s]); and • Write “No Substitution” or “No Sub” on a written prescription or indicate “No Substitution” to the pharmacist in the case of a verbal prescription. The prescriber should keep a copy of the completed form in the patient’s record for future use and reference. In the case of a written prescription, when the pharmacist or dispensing physician receives a prescription with the written notation “No Substitution” or “No Sub”, reimbursement will be provided for the higher-cost interchangeable product only if the prescription is accompanied by a completed Health Canada Side Effect Reporting Form for each of the lower-cost interchangeable drug products trialed. This form must be completely filled out noting the details of the adverse reaction and signed by the prescriber. In the case of a verbal prescription, the prescriber must satisfy the operator of the pharmacy or dispensing physician that a completed Health Canada Side Effect Reporting Form for each of the lower-cost interchangeable drug products trialed has been completed and signed by the prescriber. A written record of this verbal prescription and the completed Health Canada Side Effect Reporting Form must be received by the pharmacy prior to claim submission. Upon receipt, the pharmacist must: • Fax, submit online or mail the completed and signed form to Health Canada’s Canada Vigilance Program; and • Retain his or her copy of the completed and signed Side Effect Reporting Form. (ontario.ca, Revision #17; 2026-08-03 ↗)
Savings card: innoviCares lists Blexten (Ontario list dated 2026-09-10) — pays part of the brand-versus-generic difference after other coverage; free sign-up. (innovicares.ca ↗)
1 brand, same coverage
Blexten · DIN 02454130 Manufacturer: Aralez Pharmaceuticals Canada Inc.; listing date 2024-12-30 Health Canada: Marketed since 2019-05-30 · brand BLEXTEN · ATC R06AX29 BILASTINE · form Tablet · route Oral · ingredients BILASTINE 20 MG · company Aralez pharmaceuticals canada inc · schedule Prescription
Check this DIN again · Health Canada product record

Blexten: Formulary list price not recorded/unit (unit not stated in source; not the patient's cost)

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=94066 · Verify on the e-Formulary ↗ (DIN 02454130)

Source record
DIN 02454130: Blexten Raw flags: notABenefit=Y, sec3=Y, sec3b=Y Item: 040000089; group id 1; item number 0002; lccId None; manufacturer id ARZ Source form: Tab; strength: 20mg Recorded listing: Off-Formulary Interchangeable, not an ODB benefit Source prices (unrounded): not recorded; ministry not recorded Source: ODB odb-formulary-ed43-extract-2026-08-26.xml extract_date=2026-08-26 DIN=02454130 Health Canada DPD extract of Sep 2, 2026 (Open Government Licence – Canada) · https://health-products.canada.ca/dpd-bdpp/info?lang=eng&code=94066
Interchangeable products
Apo-Bilastine Tablets · DIN 02549883 · not recorded Auro-Bilastine · DIN 02541556 · not recorded GLN-Bilastine · DIN 02544369 · not recorded Jamp-Bilastine · DIN 02546795 · not recorded M-Bilastine · DIN 02548410 · not recorded Mar-Bilastine · DIN 02547279 · not recorded NRA-Bilastine · DIN 02551934 · not recorded PMS-Bilastine · DIN 02561565 · not recorded Sandoz Bilastine · DIN 02536269 · not recorded
Shortage status: not checked (no credentials)
Other drugs in the same formulary class (04:00 ANTIHISTAMINES) and how they are covered

Matched class: 04:00 ANTIHISTAMINES

Drug-class inventory only. Lists recorded Ontario formulary products, not every Canadian medication; does not recommend treatment. No displayed product is listed as a general benefit in this extract. Check its listing requirements below. 04:00 ANTIHISTAMINES

LORATADINE

· 2 products · Off-Formulary Interchangeable, not an ODB benefit · strengths: 10mg · Tab

RUPATADINE

· 4 products · Off-Formulary Interchangeable, not an ODB benefit · strengths: 10mg · Tab

CETIRIZINE HYDROCHLORIDE

· 21 products · Off-Formulary Interchangeable, not an ODB benefit · strengths: 10mg, 20mg · Tab Source: formulary-ed43-front-matter.txt Part V; ODB odb-formulary-ed43-extract-2026-08-26.xml extract_date=2026-08-26; class 04:00
Full class listing Related classes: Same formulary class, not same indication: class membership alone does not establish equivalent uses.
Other drugs whose Health Canada label lists a similar indication: nasal and non-nasal symptoms of seasonal allergic rhinitis
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. RUPATADINE · Off-Formulary Interchangeable, not an ODB benefit INDICATIONS AND CLINICAL USE  Allergic Rhinitis: RUPALL (rupatadine) is indicated for the symptomatic relief of nasal and non-nasal symptoms of seasonal allergic rhinitis (SAR) and perennial allergic rhinitis (PAR) in patients 2 years of age and older.  Chronic Spontaneous Urticaria: RUPALL (rupatadine) is indicated for the relief of the symptoms associated with chronic spontaneous urticaria (CSU), e.g. pruritus and hives, in patients 2 years of age and older. PM: https://pdf.hres.ca/dpd_pm/00069453.PDF; date not captured; DIN 02456451; 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 Seasonal Allergic Rhinitis JAMP BILASTINE ORAL SOLUTION (bilastine) is indicated for the symptomatic relief of nasal and non-nasal symptoms of seasonal allergic rhinitis (SAR) in patients 4 to 11 years of age with a body weight of at least 16 kg. Chronic Spontaneous Urticaria JAMP BILASTINE ORAL SOLUTION (bilastine) is indicated for the relief of the symptoms associated with chronic spontaneous urticaria (CSU) (e.g. pruritus and hives), in patients 4 to 11 years of age with a body weight of at least 16 kg. 1.1 Pediatrics Pediatrics (< 4 years of age): JAMP BILASTINE ORAL SOLUTION should not be administered to children below 4 years of age and under 16 kg due to limited data in this population. 1.2 Geriatrics Geriatrics (> 65 years of age): Not applicable. JAMP BILASTINE ORAL SOLUTION is not indicated for adults. https://pdf.hres.ca/dpd_pm/00080060.PDF PM date: not printed or not captured Source product: JAMP BILASTINE ORAL SOLUTION; DIN 02448262; fetched 2026-09-10 Product monograph posted by Health Canada; excerpt for lookup only.

Other review policies

For Blexten: no applicable EAP criteria are held and no ODB benefit is established. These policies do not establish coverage.

For rare, immediately life-, limb- or organ-threatening circumstances, the Compassionate Review Policy may consider an unfunded drug or indication, subject to its criteria and without bypassing the drug review process. Compassionate Review Policy

Compassionate Review Policy: source quote
Where there are rare clinical circumstances in immediately life, limb, or organ-threatening conditions, the Executive Officer will also consider requests for drugs or indications in situations where there has not been a decision by the Executive Officer to provide funding of the drug or indication as part of the Ontario Drug Benefit program (and the EAP), and the drug or indication requested would not circumvent the established review process for new drugs or indications as part of the drug submission process for listing within the Ontario Drug Benefit program. Requests must meet the criteria for the Compassionate Review Policy.

Ontario source; updated September 15, 2026

For cancer drugs, Case-by-Case Review considers rare, immediately life-threatening circumstances when no satisfactory funded treatment exists; its criteria and application process apply. Case-by-Case Review (cancer drugs)

Case-by-Case Review (cancer drugs): source quote
Note: Requests for cancer drugs are considered under the Case-by-Case Review Program (CBCRP) which is administered by Ontario Health (Cancer Care Ontario) on behalf of the Ministry of Health. The CBCRP considers funding requests for drugs (both oral therapies and injectable drugs) for the treatment of cancer in patients who have a rare clinical circumstance that is immediately life-threatening (death is likely within a matter of months) and who require treatment with an unfunded drug, because there is no other satisfactory and funded treatment. Please refer to the Ontario Health website for information on the application process, FAQs, eligibility criteria and program policies.

Ontario source; updated September 15, 2026