Ledum Palustre 1 X Globules ; Granules ; Liquid is a Health Canada–registered human drug (DIN 02234582) held by Dolisos Canada Inc., containing Ledum Palustre. Health Canada lists its status as Cancelled Post Market (status date 24 Apr 2006). Nexara Health has matched 17 registrations of Ledum Palustre across 3 other regulated markets, 1 of them in the same strength and dosage form.
Health Canada registration
| DIN | 02234582 |
|---|---|
| Brand name | Ledum Palustre |
| Active ingredient | Ledum Palustre |
| Strength | 1 X |
| Dosage form | Globules ; Granules ; Liquid |
| Route | Oral |
| Company | Dolisos Canada Inc. |
| Status | Cancelled Post Market — 24 Apr 2006 |
| Class | Human |
| ATC | |
| AHFS | 92:02.00* ; See footnote |
| Regulator record | Health Canada DPD entry · Product monograph |
Ledum Palustre registered in other markets
17 registrations of the same molecule in 3 national registries outside Canada (first 13 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 | Ledum palustre 7125 | Professional Complementary Health Formulas | Liquid | listed | FDA NDC | |
| Netherlands | Ledum palustre | BOIRON (Messimy) | 4 DH t/m 60 DH#2 CH t/m 200 CH#6 K t/m 100.000 K#1 LM t/m 30 LM | Globuli | Uitsluitend apotheek of drogist | EU national register |
| Netherlands | Ledum palustre | VSM Geneesmiddelen B.V. | Druppels voor oraal gebruik, oplossing | Uitsluitend apotheek of drogist | EU national register | |
| Netherlands | Ledum palustre | VSM Geneesmiddelen B.V. | Tablet | Uitsluitend apotheek of drogist | EU national register | |
| Netherlands | Ledum palustre | BOIRON (Messimy) | 4 DH t/m 60 DH#2 CH t/m 200 CH#6 K t/m 100.000 K#1 LM t/m 30 LM | Uitsluitend apotheek of drogist | EU national register | |
| United Arab Emirates | Ledum Palustre - Boiron | BOIRON, France, Messimy | MT to 200 CH | Pillules | Active | EDE |
| United States | Ledum Palustre | Hahnemann Laboratories, INC. | Pellet | listed | FDA NDC | |
| United States | Ledum Palustre | Hahnemann Laboratories, INC. | Pellet | listed | FDA NDC | |
| United States | Ledum Palustre | Hahnemann Laboratories, INC. | Pellet | listed | FDA NDC | |
| United States | Ledum Palustre | Hahnemann Laboratories, INC. | Pellet | listed | FDA NDC | |
| United States | Ledum Palustre | Hahnemann Laboratories, INC. | Pellet | listed | FDA NDC | |
| United States | Ledum Palustre | Hahnemann Laboratories, INC. | Pellet | listed | FDA NDC | |
| United States | Ledum Palustre | Hahnemann Laboratories, INC. | Pellet | listed | FDA NDC |
See every manufacturer of Ledum Palustre 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 Ledum Palustre (DIN 02234582) marketed in Canada?
No. Health Canada lists DIN 02234582 as Cancelled Post Market as of 24 Apr 2006.
Who holds the Canadian licence for this product?
Dolisos Canada Inc. is the company of record in the Health Canada Drug Product Database.
Is Ledum Palustre registered outside Canada?
Yes — Nexara Health has matched 17 registrations in 3 other markets, including 1 in the same strength and dosage form (see the table above).
Where does this data come from?
Health Canada Drug Product Database (DPD), DIN 02234582, status date 2006-04-24; national medicine registries: EDE, EU national register, 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 02234582, status date 2006-04-24; national medicine registries: EDE, EU national register, FDA NDC.
Health Canada Drug Product Database (DPD), DIN 02234582, status date 2006-04-24; national medicine registries: EDE, EU national register, FDA NDC. Last reviewed 2026-09-17. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.