Podophyllum-Injeel Liq (12d,30d,200d/1.1ml) 12 D / 1.1 mL Liquid is a Health Canada–registered human drug (DIN 02068842) held by Biologische Heilmittel Heel GmbH, containing Podophyllum. Health Canada lists its status as Cancelled Post Market (status date 31 Jul 2009). Nexara Health has matched 12 registrations of Podophyllum across 1 other regulated market.
Health Canada registration
| DIN | 02068842 |
|---|---|
| Brand name | Podophyllum-Injeel Liq (12d,30d,200d/1.1ml) |
| Active ingredient | Podophyllum |
| Strength | 12 D / 1.1 mL |
| Dosage form | Liquid |
| Route | Oral |
| Company | Biologische Heilmittel Heel GmbH |
| Status | Cancelled Post Market — 31 Jul 2009 |
| Class | Human |
| ATC | |
| AHFS | 92:02.00* ; See footnote |
| Regulator record | Health Canada DPD entry · Product monograph |
Podophyllum registered in other markets
12 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 | Bestmade Natural Products Podophyllum | Bestmade Natural Products | Tablet, Soluble | listed | FDA NDC | |
| United States | BM Podophyllum | BM Private Limited | Globule | listed | FDA NDC | |
| United States | Podophyllum Pelt Kit Refill | Washington Homeopathic Products | Pellet | listed | FDA NDC | |
| United States | Podophyllum peltatum | Boiron | Pellet | listed | FDA NDC | |
| United States | Podophyllum peltatum | Boiron | Pellet | listed | FDA NDC | |
| United States | Podophyllum peltatum | Boiron | Pellet | listed | FDA NDC | |
| United States | Podophyllum peltatum | Boiron | Pellet | listed | FDA NDC | |
| United States | Podophyllum peltatum | Boiron | Pellet | listed | FDA NDC |
See every manufacturer of Podophyllum 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 Podophyllum-Injeel Liq (12d,30d,200d/1.1ml) (DIN 02068842) marketed in Canada?
No. Health Canada lists DIN 02068842 as Cancelled Post Market as of 31 Jul 2009.
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 Podophyllum registered outside Canada?
Yes — Nexara Health has matched 12 registrations in 1 other market (see the table above).
Where does this data come from?
Health Canada Drug Product Database (DPD), DIN 02068842, status date 2009-07-31; 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 02068842, status date 2009-07-31; national medicine registries: FDA NDC.
Health Canada Drug Product Database (DPD), DIN 02068842, status date 2009-07-31; 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.