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ATOVAQUONE

All products: general benefit

GLN-Atovaquone · DIN 02528495 · 750mg/5mL · oral liquid

General benefitMarketed · checked 2026-09-02
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.
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 ↗)
1 brand, same coverage
GLN-Atovaquone · DIN 02528495 Manufacturer: Glenmark Pharmaceuticals Canada Inc.; listing date 2022-10-31 Health Canada: Marketed since 2022-06-30 · brand GLN-ATOVAQUONE · ATC P01AX06 ATOVAQUONE · form Suspension · route Oral · ingredients ATOVAQUONE 750 MG/5ML · company Glenmark pharmaceuticals canada inc. · schedule Prescription
Check this DIN again · Health Canada product record

Ministry pays: $1.5856 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=101772 · Verify on the e-Formulary ↗ (DIN 02528495)

Source record
DIN 02528495: GLN-Atovaquone Raw flags: sec3=Y Item: 083000001; group id 124; item number 0208; lccId None; manufacturer id GLP Source form: O/L; strength: 750mg/5mL Recorded listing: General benefit Source prices (unrounded): $1.5857; ministry $1.5856 Source: ODB odb-formulary-ed43-extract-2026-08-26.xml extract_date=2026-08-26 DIN=02528495 Health Canada DPD extract of Sep 2, 2026 (Open Government Licence – Canada) · https://health-products.canada.ca/dpd-bdpp/info?lang=eng&code=101772
Interchangeable products
Auro-Atovaquone · DIN 02556618 · $1.5856 Mepron · DIN 02217422 · $1.5856
Shortage status: resolved shortage (ended 2024-10-16); reports as of 2026-09-13T08:10:21.292534+00:00 (Health Product Shortages Canada) Source: https://healthproductshortages.ca/search?term=02528495
Shortage record checked 2026-09-13T08:10:21.292534+00:00
Other drugs in the same formulary class (08:30 Antiprotozoals) and how they are covered
No products matched this class search: “08:30”. This is a search result, not a decision about coverage. Try a different class name, abbreviation or class code. Search this as a medication name or DIN
Full class listing Related classes: 08:08 Anthelmintics, 08:12 Antibiotics, 08:14 Antifungals, 08:16 Antitubercular Agents, 08:18 Antivirals, 08:20 Plasmodicides (Antimalarials), 08:24 Sulfonamides, 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.
What the Health Canada label says it is for
1. Indications MEPRON (atovaquone) Oral Suspension is indicated for: • the acute oral treatment of mild to moderate Pneumocystis jirovecii pneumonia (PCP) in patients who are intolerant to trimethoprim-sulfamethoxazole (TMP-SMX). 1.1. Pediatrics There are no efficacy studies in children. Clinical experience with MEPRON (atovaquone) in immunosuppressed pediatric patients is limited to safety data from one pharmacokinetic study (n = 11). No children under 4 months of age participated in the Phase I trial. 1.2. Geriatrics MEPRON (atovaquone) has not been systematically evaluated in patients greater than 65 years of age. Caution should be exercised when treating elderly patients reflecting the greater frequency of decreased hepatic, renal and cardiac function in this population. https://pdf.hres.ca/dpd_pm/00083946.PDF PM date: 2026-03-05 Source product: MEPRON; DIN 02217422; fetched 2026-09-10 Product monograph posted by Health Canada; excerpt for lookup only.