LUPRON DIN 00727695
Status: Cancelled Post Market
Holder: ABBVIE CORPORATION
Molecule: LEUPROLIDE ACETATE
Available to quote
Health Canada record
| Active ingredient(s) | LEUPROLIDE ACETATE 5 MG |
|---|---|
| Dosage form | Solution |
| Route | Subcutaneous |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | L02AE02 LEUPRORELIN |
| Original market date | 31-Dec-1985 |
| Current status date | 14-Sep-2022 |
| Source | Health Canada DPD |
Establishment licence of the holder
AbbVie Corporation — licence 101988, currently licensed, last inspection rating C (2023-07-18).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing LEUPROLIDE ACETATE
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02248999 | ELIGARD | TOLMAR INTERNATIONAL LTD. | Powder For Suspension (Sustained-Release | LEUPROLIDE ACETATE 30 MG | Marketed |
| 02268892 | ELIGARD | TOLMAR INTERNATIONAL LTD. | Powder For Suspension (Sustained-Release | LEUPROLIDE ACETATE 45 MG | Marketed |
| 02248240 | ELIGARD | TOLMAR INTERNATIONAL LTD. | Powder For Suspension (Sustained-Release | LEUPROLIDE ACETATE 22.5 MG | Marketed |
| 02248239 | ELIGARD | TOLMAR INTERNATIONAL LTD. | Powder For Suspension (Sustained-Release | LEUPROLIDE ACETATE 7.5 MG | Marketed |
| 02239834 | LUPRON DEPOT | ABBVIE CORPORATION | Powder For Suspension (Sustained-Release | LEUPROLIDE ACETATE 11.25 MG | Marketed |
| 00836273 | LUPRON DEPOT | ABBVIE CORPORATION | Powder For Suspension (Sustained-Release | LEUPROLIDE ACETATE 7.5 MG | Marketed |
| 00884502 | LUPRON DEPOT | ABBVIE CORPORATION | Powder For Suspension (Sustained-Release | LEUPROLIDE ACETATE 3.75 MG | Marketed |
| 02230248 | LUPRON DEPOT | ABBVIE CORPORATION | Powder For Suspension (Sustained-Release | LEUPROLIDE ACETATE 22.5 MG | Marketed |
| 02239833 | LUPRON DEPOT | ABBVIE CORPORATION | Powder For Suspension (Sustained-Release | LEUPROLIDE ACETATE 30 MG | Marketed |
| 02562855 | LUPRON DEPOT | ABBVIE CORPORATION | Powder For Suspension (Sustained-Release | LEUPROLIDE ACETATE 45 MG | Marketed |
| 02429977 | ZEULIDE DEPOT | VERITY PHARMACEUTICALS INC. | Kit; Powder For Suspension (Sustained-Release | LEUPROLIDE ACETATE 3.75 MG | Marketed |
| 02462699 | ZEULIDE DEPOT | VERITY PHARMACEUTICALS INC. | Kit; Powder For Suspension (Sustained-Release | LEUPROLIDE ACETATE 22.5 MG | Marketed |
| 02240264 | LEUPROLIDE ACETATE INJECTION | NOVOPHARM LIMITED | Liquid | LEUPROLIDE ACETATE 5 MG | Cancelled Pre Market |
| 02148730 | LUPRON DEPOT | ABBVIE CORPORATION | Powder For Suspension (Sustained-Release | LEUPROLIDE ACETATE 15 MG | Cancelled Pre Market |
| 02148722 | LUPRON DEPOT | ABBVIE CORPORATION | Powder For Suspension (Sustained-Release | LEUPROLIDE ACETATE 11.25 MG | Cancelled Pre Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 13812 | 2012-11-02 | New Drug Submission (NDS) | Manufacturer name change |
| 9855 | 2008-10-24 | New Drug Submission (NDS) | MANUFACTURER NAME CHANGE |
| 9856 | 2008-10-24 | New Drug Submission (NDS) | MANUFACTURER NAME CHANGE |
International API supply for LEUPROLIDE ACETATE
13 active FDA Drug Master Files.
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