FERTILINE DIN 02030314
Health Canada record
| Active ingredient(s) | GONADORELIN ACETATE 50 MCG |
|---|---|
| Dosage form | Solution |
| Route | Intramuscular |
| Schedule | PRESCRIPTION |
| Class | Veterinary |
| ATC | |
| Original market date | 31-Dec-1993 |
| Current status date | 13-Sep-2000 |
| Source | Health Canada DPD |
Establishment licence of the holder
Vetoquinol N A Inc. — licence 100448, currently licensed, last inspection rating C (2025-10-20).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing GONADORELIN ACETATE
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02496763 | GONABREED | PARNELL TECHNOLOGIES PTY LTD | Solution | GONADORELIN ACETATE 100 MCG | Marketed |
| 02046202 | LUTREPULSE | FERRING INC | Powder For Solution | GONADORELIN ACETATE 3.2 MG | Dormant |
| 02046210 | LUTREPULSE PWS 0.8MG/VIAL | FERRING INC | Powder For Solution | GONADORELIN ACETATE 0.8 MG | Cancelled Post Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 33261 | 2024-05-17 | Supplement to a New Drug Submission (SNDS) | Alternate drug product batch size and related manufacturing changes |
| 19924 | 2017-10-18 | Supplement to a New Drug Submission (SNDS) | CHANGE IN WITHDRAWAL PERIOD |
| 8775 | 2007-05-10 | Supplement to a New Drug Submission (SNDS) | CHANGE IN WITHDRAWAL PERIOD |
| 6487 | 2000-02-14 | New Drug Submission (NDS) |
International API supply for GONADORELIN ACETATE
4 valid EDQM Certificates of Suitability from 4 holders. 2 active FDA Drug Master Files.
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