Foquest · DIN 02470306 · 35mg · CR capsule
General benefitMarketed · checked 2026-09-20
StatusGeneral benefit
Write on scriptno code needed
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.
No interchangeable product listed in the Ontario extract
Foquest · DIN 02470306
Manufacturer: Elvium Life Sciences; listing date 2023-04-28
Health Canada: Marketed since 2020-09-08 · brand FOQUEST · ATC N06BA04 METHYLPHENIDATE · form Capsule (controlled-release) · route Oral · ingredients METHYLPHENIDATE HYDROCHLORIDE 35 MG · company Elvium life sciences · schedule Controlled drugs (cdsa iii)
Foquest: Formulary list price $3.3388/unit (unit not stated in source; not the patient's cost)
Ministry pays: $3.3388 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=95928 · Verify on the e-Formulary ↗ (DIN 02470306)
Source record
DIN 02470306: Foquest
Raw flags: sec3=Y
Item: 282000081; group id 516; item number 1378; lccId None; manufacturer id ELV
Source form: CR Cap; strength: 35mg
Recorded listing: General benefit
Source prices (unrounded): $3.3388; ministry $3.3388
Source: ODB odb-formulary-ed43-extract-2026-08-26.xml extract_date=2026-08-26 DIN=02470306
Health Canada DPD extract of Sep 2, 2026 (Open Government Licence – Canada) · https://health-products.canada.ca/dpd-bdpp/info?lang=eng&code=95928
Therapeutic Notes (formulary)
Notes: Patients greater than or equal to 6 years of age diagnosed with ADHD according to DSM-IV criteria and where symptoms are not due to other medical conditions which affect concentration, and who require 12-hour continuous coverage due to academic and/or psychosocial needs, and who meet the following:
1) Patients who demonstrate significant and problematic disruptive behaviour or who have problems with inattention that interfere with learning AND
2) Prescribed by or in consultation with a specialist in pediatric psychiatry, pediatrics or a general practitioner with expertise in ADHD AND
3) Have been tried on methylphenidate immediate release (IR) or methylphenidate slow release (SR) or Dexedrine IR or Dexedrine SR (Spansules), and have experienced unsatisfactory results due to poor symptom control, side effects, administrative barriers, or societal barriers.
Administrative barriers include:
- inability of a school to dose the child at lunch;
- the school lunch hour does not coincide with the dosing schedule;
- poor compliance with noon or afternoon doses;
- the patient is unable to swallow tablets.
Societal barriers include:
- the patient or patient's caregiver(s) has/have a history of substance abuse or diversion of listed immediate-release alternatives;
- the patient or patient's caregiver(s) is/are at risk of substance abuse or diversion of listed immediate-release alternatives.
Shortage status: not checked (no credentials)