REKOVELLE DIN 02487470
Status: Marketed
Holder: FERRING INC
Available to quote
Health Canada record
| Active ingredient(s) | FOLLITROPIN DELTA 36 MCG |
|---|
| Dosage form | Solution |
|---|
| Route | Subcutaneous |
|---|
| Schedule | SCHEDULE D; PRESCRIPTION |
|---|
| Class | Human |
|---|
| ATC | G03GA10 FOLLITROPIN DELTA |
|---|
| Original market date | 01-Nov-2019 |
|---|
| Current status date | 01-Nov-2019 |
|---|
| Source | Health Canada DPD |
|---|
Establishment licence of the holder
Ferring Inc. — licence 100274, currently licensed, last inspection rating C (2026-05-19).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing FOLLITROPIN DELTA
| DIN | Product | Company | Form | Strength | Status |
|---|
| 02487462 | REKOVELLE | FERRING INC | Solution | FOLLITROPIN DELTA 12 MCG | Marketed |
| 02487489 | REKOVELLE | FERRING INC | Solution | FOLLITROPIN DELTA 72 MCG | Marketed |
| 02474077 | REKOVELLE | FERRING INC | Solution | FOLLITROPIN DELTA 72 MCG | Cancelled Post Market |
| 02474085 | REKOVELLE | FERRING INC | Solution | FOLLITROPIN DELTA 36 MCG | Cancelled Post Market |
| 02474093 | REKOVELLE | FERRING INC | Solution | FOLLITROPIN DELTA 12 MCG | Cancelled Post Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|
| 22075 | 2019-04-18 | Supplement to a New Drug Submission (SNDS) | NEW PRESENTATION |
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