Vaginex W Tripelennamine Crm 2% 2 % Cream is a Health Canada–registered human drug (DIN 00584096) held by Julius Schmid Canada Ltd., containing Tripelennamine Hydrochloride. Health Canada lists its status as Cancelled Post Market (status date 07 Aug 1997). Nexara Health has matched 19 registrations of Tripelennamine Hydrochloride across 4 other regulated markets.
Health Canada registration
| DIN | 00584096 |
|---|---|
| Brand name | Vaginex W Tripelennamine Crm 2% |
| Active ingredient | Tripelennamine Hydrochloride |
| Strength | 2 % |
| Dosage form | Cream |
| Route | Vaginal |
| Company | Julius Schmid Canada Ltd. |
| Status | Cancelled Post Market — 07 Aug 1997 |
| Class | Human |
| ATC | |
| AHFS | 04:04.08 |
| Regulator record | Health Canada DPD entry · Product monograph |
Tripelennamine Hydrochloride registered in other markets
19 registrations of the same molecule in 4 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 |
|---|---|---|---|---|---|---|
| Finland | Etono | Perrigo Sverige AB | 20 mg/g | ihopuikko | Myyntilupa myönnetty | Fimea Perusrekisteri |
| Finland | Vetibenzamin Vet | Novartis Pharma Stein AG | 20 mg/ml | injektioneste | Myyntilupa peruuntunut | Fimea Perusrekisteri |
| Netherlands | Azaron Stick, stift 20 mg/g | Omega Pharma Nederland B.V. | Huidstift | Algemene verkoop [conform voorwaarden CBG AV-lijst d.d. 6 september 2007] | EU national register | |
| Netherlands | Azaron, crème 20 mg/g | Omega Pharma Nederland B.V. | Crème | Algemene verkoop [conform voorwaarden CBG AV-lijst d.d. 6 september 2007] | EU national register | |
| Taiwan | Ipelennamine HCl Tablets "Jen Sheng" | 人生製藥股份有限公司 | 錠劑 | 已註銷 | TFDA | |
| Taiwan | Tripelennamine Hc1 Tablets "Chi Sheng" | 濟生化學製藥廠股份有限公司 | 錠劑 | 已註銷 | TFDA | |
| Taiwan | Tripelennamine Hc1 Tablets 50mg "Johnson" | 強生化學製藥廠有限公司 | 錠劑 | 已註銷 | TFDA | |
| Taiwan | Tripelennamine HCl | Dolder Ltd. | （粉） | 已註銷 | TFDA | |
| Taiwan | Tripelennamine HCl | Internazionale Farmaceutical S. P. A. | （粉） | 已註銷 | TFDA | |
| Taiwan | Tripelennamine HCl | Wander Chemical Ltd. | （粉） | 已註銷 | TFDA | |
| Taiwan | Tripelennamine HCl | Archemia S.p.a. | （粉） | 已註銷 | TFDA | |
| Taiwan | Tripelennamine HCl | Internazionale Farmaceutical S. P. A. | （粉） | 已註銷 | TFDA | |
| United States | Tripelennamine Hydrochloride | Kingchem Laboratories Inc. | Powder | FDA NDC |
See every manufacturer of Tripelennamine Hydrochloride 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 Vaginex W Tripelennamine Crm 2% (DIN 00584096) marketed in Canada?
No. Health Canada lists DIN 00584096 as Cancelled Post Market as of 07 Aug 1997.
Who holds the Canadian licence for this product?
Julius Schmid Canada Ltd. is the company of record in the Health Canada Drug Product Database.
Is Tripelennamine Hydrochloride registered outside Canada?
Yes — Nexara Health has matched 19 registrations in 4 other markets (see the table above).
Where does this data come from?
Health Canada Drug Product Database (DPD), DIN 00584096, status date 1997-08-07; national medicine registries: EU national register, FDA NDC, Fimea Perusrekisteri, TFDA. 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 00584096, status date 1997-08-07; national medicine registries: EU national register, FDA NDC, Fimea Perusrekisteri, TFDA.
Health Canada Drug Product Database (DPD), DIN 00584096, status date 1997-08-07; national medicine registries: EU national register, FDA NDC, Fimea Perusrekisteri, TFDA. Last reviewed 2026-09-17. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.