Heel-080 Tablets 6 Dh Tablet is a Health Canada–registered human drug (DIN 01969102) held by Biologische Heilmittel Heel GmbH, containing Antimony Trisulfide. Health Canada lists its status as Cancelled Post Market (status date 30 Jan 1998). Nexara Health has matched 11 registrations of Antimony Trisulfide across 1 other regulated market.
Health Canada registration
| DIN | 01969102 |
|---|---|
| Brand name | Heel-080 Tablets |
| Active ingredient | Antimony Trisulfide |
| Strength | 6 Dh |
| Dosage form | Tablet |
| Route | Oral |
| Company | Biologische Heilmittel Heel GmbH |
| Status | Cancelled Post Market — 30 Jan 1998 |
| Class | Human |
| ATC | |
| AHFS | |
| Regulator record | Health Canada DPD entry · Product monograph |
Antimony Trisulfide registered in other markets
11 registrations of the same molecule in 1 national registry outside Canada (first 8 shown, exact strength and form first). Each row is taken from the regulator's own published list; status is shown as the registry reports it.
| Country | Product | Marketing authorisation holder | Strength | Form | Status | Registry |
|---|---|---|---|---|---|---|
| United States | Antimonium crudum | Boiron | Pellet | listed | FDA NDC | |
| United States | Antimonium crudum | Boiron | Pellet | listed | FDA NDC | |
| United States | Antimonium crudum | Boiron | Pellet | listed | FDA NDC | |
| United States | Antimonium crudum | Boiron | Pellet | listed | FDA NDC | |
| United States | Antimonium crudum | Boiron | Pellet | listed | FDA NDC | |
| United States | Antimonium crudum | Boiron | Pellet | listed | FDA NDC | |
| United States | Antimonium crudum | Boiron | Pellet | listed | FDA NDC | |
| United States | Antimonium crudum | Boiron | Pellet | listed | FDA NDC |
See every manufacturer of Antimony Trisulfide worldwide →
Sourcing through Nexara Health
Nexara Health is a Health Canada–licensed wholesaler (DEL #3-002896) in Winnipeg. This DIN is not currently marketed in Canada. The registrations above show which regulated markets hold an equivalent presentation that can be sourced for clinical comparator use or on a named-patient basis under Health Canada's Special Access Programme. Request a quote or read how named-patient and foreign-pack supply works in Canada.
Frequently asked questions
Is Heel-080 Tablets (DIN 01969102) marketed in Canada?
No. Health Canada lists DIN 01969102 as Cancelled Post Market as of 30 Jan 1998.
Who holds the Canadian licence for this product?
Biologische Heilmittel Heel GmbH is the company of record in the Health Canada Drug Product Database.
Is Antimony Trisulfide registered outside Canada?
Yes — Nexara Health has matched 11 registrations in 1 other market (see the table above).
Where does this data come from?
Health Canada Drug Product Database (DPD), DIN 01969102, status date 1998-01-30; national medicine registries: FDA NDC. Nexara Health re-checks these sources weekly and shows the last verification date at the top of the page.
Source: Health Canada Drug Product Database (DPD), DIN 01969102, status date 1998-01-30; national medicine registries: FDA NDC.
Health Canada Drug Product Database (DPD), DIN 01969102, status date 1998-01-30; national medicine registries: FDA NDC. Last reviewed 2026-09-16. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.