Cubeba-Injeel Liq (10d,30d,200d/1.1ml) 10 D / 1.1 mL Liquid is a Health Canada–registered human drug (DIN 02053845) held by Biologische Heilmittel Heel GmbH, containing Cubeba Officinalis. Health Canada lists its status as Cancelled Post Market (status date 17 Jan 1997). Nexara Health has matched 8 registrations of Cubeba Officinalis across 1 other regulated market.
Health Canada registration
| DIN | 02053845 |
|---|---|
| Brand name | Cubeba-Injeel Liq (10d,30d,200d/1.1ml) |
| Active ingredient | Cubeba Officinalis |
| Strength | 10 D / 1.1 mL |
| Dosage form | Liquid |
| Route | Oral |
| Company | Biologische Heilmittel Heel GmbH |
| Status | Cancelled Post Market — 17 Jan 1997 |
| Class | Human |
| ATC | |
| AHFS | 92:02.00* ; See footnote |
| Regulator record | Health Canada DPD entry · Product monograph |
Cubeba Officinalis registered in other markets
8 registrations of the same molecule in 1 national registry outside Canada. 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 | Cubeba Officinalis | Hahnemann Laboratories, INC. | Pellet | listed | FDA NDC | |
| United States | Cubeba Officinalis | Hahnemann Laboratories, INC. | Pellet | listed | FDA NDC | |
| United States | Cubeba Officinalis | Hahnemann Laboratories, INC. | Pellet | listed | FDA NDC | |
| United States | Cubeba Officinalis | Hahnemann Laboratories, INC. | Pellet | listed | FDA NDC | |
| United States | Cubeba Officinalis | Hahnemann Laboratories, INC. | Pellet | listed | FDA NDC | |
| United States | Cubeba Officinalis | Hahnemann Laboratories, INC. | Pellet | listed | FDA NDC | |
| United States | Cubeba Officinalis | Hahnemann Laboratories, INC. | Pellet | listed | FDA NDC | |
| United States | Cubeba Officinalis | Hahnemann Laboratories, INC. | Pellet | listed | FDA NDC |
See every manufacturer of Cubeba Officinalis 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 Cubeba-Injeel Liq (10d,30d,200d/1.1ml) (DIN 02053845) marketed in Canada?
No. Health Canada lists DIN 02053845 as Cancelled Post Market as of 17 Jan 1997.
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 Cubeba Officinalis registered outside Canada?
Yes — Nexara Health has matched 8 registrations in 1 other market (see the table above).
Where does this data come from?
Health Canada Drug Product Database (DPD), DIN 02053845, status date 1997-01-17; 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 02053845, status date 1997-01-17; national medicine registries: FDA NDC.
Health Canada Drug Product Database (DPD), DIN 02053845, status date 1997-01-17; 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.