Drug · DIN 02148633
DUOVENT UDV
No: no longer authorized
The company stopped selling it and its DIN was cancelled. A cancellation is most often a business decision; the record does not say why.
Status Cancelled Post Market since January 31, 2017; first marketed December 31, 1995.
- Drug Identification Number (DIN)
- 02148633
- Company (DIN owner)
- Boehringer Ingelheim (Canada) Ltd.Burlington, Ontario, Canada
- Schedule
- Prescription
- Dosage form
- Solution
- Route
- Oral; Inhalation
- Therapeutic class (ATC)
- Fenoterol and ipratropium bromide R03AL01
- Class
- Human
- Record last updated
- June 17, 2026
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| IPRATROPIUM BROMIDE | 0.125 MG | ML |
| FENOTEROL HYDROBROMIDE | 0.3125 MG | ML |
Notices of Compliance
Health Canada approvals that name this DIN.
- January 12, 1995: NOC 4759New Drug Submission (NDS)