Drug · DIN 02445301
PERGOVERIS
R-HFSH: 11 MCG - R-HLH: 3 MCG/VIAL, AND DILUENT
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 July 4, 2019; first marketed October 22, 2015.
- Drug Identification Number (DIN)
- 02445301
- Company (DIN owner)
- Emd Serono A Division Of Emd Inc CanadaMississauga, Ontario, Canada
- Schedule
- Schedule D; Prescription
- Dosage form
- Kit; Powder For Solution
- Route
- Subcutaneous
- Therapeutic class (ATC)
- Combinations G03GA30
- Class
- Human
- Record last updated
- August 6, 2026
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| FOLLITROPIN ALFA | 150 UNIT | VIAL |
| LUTROPIN ALFA | 75 UNIT | VIAL |
Notices of Compliance
Health Canada approvals that name this DIN.
- August 25, 2015: NOC 17226New Drug Submission (NDS)
Other DINs named PERGOVERIS
- DIN 02470640 · Marketed
- DIN 02470659 · Marketed
- DIN 02470667 · Marketed