Medication
Diltiazem CD
DIN 02400421 · Sanis Health Inc
What it is
- Active ingredients
- Diltiazem Hydrochloride — 120 mg
- Form and route
- Capsule (Controlled-Delivery) · Oral
- Schedule
- PRESCRIPTION
- Authorised since
- 2013-02-13
Source: Health Canada — Drug Product Database. Data current as of 2026-08-12.
Products with the same active ingredient
- Apo-Diltiaz CD
- Tiazac
- Teva-Diltiazem CD
- Tiazac XC
- Teva-Diltiazem T
- Diltiazem CD
- Mar-Diltiazem T
- Mar-Diltiazem CD
- Jamp Diltiazem T
- Diltiazem T
- Jamp Diltiazem CD
- Pro-Diltiazem CD
- M-Diltiazem CD
- M-Diltiazem T
Grouped by Health Canada’s active-ingredient group number. Products in a group do not always share a strength — check the strength above against your own. Sharing an active ingredient does not mean two products can be substituted for each other: whether a substitution is permitted is a provincial decision, and this page does not show it. Ask a pharmacist.
Watch this medication
Ontario Drug Benefit coverage
As of 31 July 2026General benefit Part III-A
Ontario lists this product as a general benefit under the Ontario Drug Benefit program — Part III-A of the Formulary/CDI. For someone eligible for ODB, it is covered without a drug-specific approval.
- What ODB pays per unit
- $0.3634
This is what the Ontario Drug Benefit program reimburses a pharmacy for one unit, as of 31 July 2026. A deductible and a co-payment sit on top of it and differ by program — ODB, the Trillium Drug Program and the seniors co-payment each work differently — so it is not the figure anyone is charged at a counter. It also says nothing about private, workplace or federal coverage.
Source: Ontario Ministry of Health — ODB Formulary. Data current as of 2026-07-28. Ontario only. Formulary edition 4342, effective 31 July 2026.
Products Ontario considers interchangeable
As of 31 July 2026Ontario groups these products together at 120mg LA Cap and will substitute one for another at a pharmacy counter in Ontario.
- Apo-Diltiaz CD 02230997Apotex Inc
- Diltiazem CD 02445999Sivem Pharmaceuticals ULC
- Jamp Diltiazem CD 02528037Jamp Pharma Corporation
- M-Diltiazem CD 02546086Mantra Pharma Inc
- Mar-Diltiazem CD 02484064Marcan Pharmaceuticals Inc
- Teva-Diltiazem CD 02242538Teva Canada Limited
Ontario lists 3 further products in this group that are not currently marketed in Canada. They are not shown.
This is Ontario’s designation, under the Ontario Drug Benefit program, and it applies in Ontario. It is a different statement from the same-active-ingredient list above, which is Health Canada’s grouping and carries no substitution meaning at all. No other province’s rules are shown on this page, and a designation here is not a recommendation to switch — that is a conversation with a pharmacist or prescriber.
Source: Ontario Ministry of Health — ODB Formulary. Data current as of 2026-07-28. Ontario only. Formulary edition 4342, effective 31 July 2026.
How it is classified
- Anatomical main group
- Cardiovascular system
- ATC code
- C08DB01
The Anatomical Therapeutic Chemical code records the body system a medicine acts on and its chemical grouping. It is not a statement of what this medication treats, and nothing on this page is. For the full classification of C08DB01, see the WHO ATC/DDD Index.
Recalls and safety alerts
As of 12 August 2026Archived by Health Canada
2 older notices naming this product have been archived. These are a record of what happened, not current warnings.
Diltiazem-CD 300 mg capsules (2014-02-20)
Possible match. This notice names “DILTIAZEM CD”, and 8 authorised products from 2 companies are sold under that name. The notice does not say which of them is affected.
Possible match. This notice names “DILTIAZEM CD”, and 8 authorised products from 2 companies are sold under that name. The notice does not say which of them is affected.
This list may be incomplete. Health Canada’s recalls data carries no DIN, so notices are matched on wording alone. Search Health Canada recalls for Diltiazem CD → How RxMonitor matches recalls, and how often it fails
Source: Health Canada — Recalls and Safety Alerts. Data current as of 2026-08-12. Matched on product name, not on DIN — the feed carries none.