Drug · DIN 02046202
LUTREPULSE
Authorized, but not sold for a year or more
Authorized, but the company reports it has not been sold in Canada for at least 12 months.
Status Dormant since April 21, 2017; first marketed December 31, 1994.
- Drug Identification Number (DIN)
- 02046202
- Company (DIN owner)
- Ferring Inc.North York, Ontario, Canada
- Schedule
- Prescription
- Dosage form
- Powder For Solution
- Route
- Intravenous; Subcutaneous
- Therapeutic class (ATC)
- Gonadorelin H01CA01
- Class
- Human
- Record last updated
- August 6, 2026
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| GONADORELIN ACETATE | 3.2 MG | VIAL |
Notices of Compliance
Health Canada approvals that name this DIN.
- August 27, 2010: NOC 11693Supplement to a New Drug Submission (SNDS) · Reactivation of the 3.2 mg strength