OCTREOTIDE ACETATE INJECTION - 50MCG/ML DIN 02263165
Status: Cancelled Pre Market
Holder: SANDOZ CANADA INCORPORATED
Molecule: OCTREOTIDE (OCTREOTIDE ACETATE)
Health Canada record
| Active ingredient(s) | OCTREOTIDE (OCTREOTIDE ACETATE) 50 MCG |
|---|---|
| Dosage form | Solution |
| Route | Intravenous; Subcutaneous |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | H01CB02 OCTREOTIDE |
| Original market date | |
| Current status date | 01-Aug-2019 |
| Source | Health Canada DPD |
Establishment licence of the holder
Sandoz Canada Incorporated — licence 101370, currently licensed, last inspection rating C (2025-02-25).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing OCTREOTIDE (OCTREOTIDE ACETATE)
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02509776 | OCTREOTIDE ACETATE INJECTION | GENERIC MEDICAL PARTNERS INC | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 500 MCG | Approved |
| 02509768 | OCTREOTIDE ACETATE INJECTION | GENERIC MEDICAL PARTNERS INC | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 100 MCG | Approved |
| 02509741 | OCTREOTIDE ACETATE INJECTION | GENERIC MEDICAL PARTNERS INC | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 50 MCG | Approved |
| 02248642 | OCTREOTIDE ACETATE OMEGA | OMEGA LABORATORIES LIMITED | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 200 MCG | Marketed |
| 02248639 | OCTREOTIDE ACETATE OMEGA | OMEGA LABORATORIES LIMITED | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 50 MCG | Marketed |
| 02248640 | OCTREOTIDE ACETATE OMEGA | OMEGA LABORATORIES LIMITED | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 100 MCG | Marketed |
| 02248641 | OCTREOTIDE ACETATE OMEGA | OMEGA LABORATORIES LIMITED | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 500 MCG | Marketed |
| 02567792 | OCTREOTIDE DEPOT | STERIMAX INC | Powder For Suspension (Sustained-Release | OCTREOTIDE (OCTREOTIDE ACETATE) 30 MG | Marketed |
| 02567784 | OCTREOTIDE DEPOT | STERIMAX INC | Powder For Suspension (Sustained-Release | OCTREOTIDE (OCTREOTIDE ACETATE) 20 MG | Marketed |
| 02567776 | OCTREOTIDE DEPOT | STERIMAX INC | Powder For Suspension (Sustained-Release | OCTREOTIDE (OCTREOTIDE ACETATE) 10 MG | Marketed |
| 02560240 | OCTREOTIDE INJECTION | STERIMAX INC | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 100 MCG | Marketed |
| 02535920 | OCTREOTIDE INJECTION | MONT-PHARMA INC | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 500 MCG | Approved |
| 02535912 | OCTREOTIDE INJECTION | MONT-PHARMA INC | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 200 MCG | Approved |
| 02535890 | OCTREOTIDE INJECTION | MONT-PHARMA INC | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 50 MCG | Approved |
| 02535904 | OCTREOTIDE INJECTION | MONT-PHARMA INC | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 100 MCG | Approved |
| 02560291 | OCTREOTIDE INJECTION | STERIMAX INC | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 500 MCG | Marketed |
| 02560283 | OCTREOTIDE INJECTION | STERIMAX INC | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 200 MCG | Marketed |
| 00839191 | SANDOSTATIN | NOVARTIS PHARMACEUTICALS CANADA INC | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 50 MCG | Marketed |
| 02239323 | SANDOSTATIN LAR | NOVARTIS PHARMACEUTICALS CANADA INC | Powder For Suspension (Sustained-Release | OCTREOTIDE (OCTREOTIDE ACETATE) 10 MG | Marketed |
| 02239324 | SANDOSTATIN LAR | NOVARTIS PHARMACEUTICALS CANADA INC | Powder For Suspension (Sustained-Release | OCTREOTIDE (OCTREOTIDE ACETATE) 20 MG | Marketed |
| 02239325 | SANDOSTATIN LAR | NOVARTIS PHARMACEUTICALS CANADA INC | Powder For Suspension (Sustained-Release | OCTREOTIDE (OCTREOTIDE ACETATE) 30 MG | Marketed |
| 02413191 | OCPHYL | PENDOPHARM DIVISION OF PHARMASCIENCE INC | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 50 MCG | Cancelled Post Market |
| 02413205 | OCPHYL | PENDOPHARM DIVISION OF PHARMASCIENCE INC | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 100 MCG | Cancelled Post Market |
| 02413213 | OCPHYL | PENDOPHARM DIVISION OF PHARMASCIENCE INC | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 500 MCG | Cancelled Post Market |
| 02263173 | OCTREOTIDE ACETATE INJECTION - 100MCG/ML | SANDOZ CANADA INCORPORATED | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 100 MCG | Cancelled Pre Market |
| 02263181 | OCTREOTIDE ACETATE INJECTION - 200MCG/ML | SANDOZ CANADA INCORPORATED | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 200 MCG | Cancelled Pre Market |
| 02263203 | OCTREOTIDE ACETATE INJECTION - 500MCG/ML | SANDOZ CANADA INCORPORATED | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 500 MCG | Cancelled Pre Market |
| 02503786 | OCTREOTIDE FOR INJECTABLE SUSPENSION | TEVA CANADA LIMITED | Powder For Suspension (Sustained-Release; Kit | OCTREOTIDE (OCTREOTIDE ACETATE) 30 MG | Cancelled Post Market |
| 02503751 | OCTREOTIDE FOR INJECTABLE SUSPENSION | TEVA CANADA LIMITED | Kit; Powder For Suspension (Sustained-Release | OCTREOTIDE (OCTREOTIDE ACETATE) 10 MG | Cancelled Post Market |
| 02503778 | OCTREOTIDE FOR INJECTABLE SUSPENSION | TEVA CANADA LIMITED | Kit; Powder For Suspension (Sustained-Release | OCTREOTIDE (OCTREOTIDE ACETATE) 20 MG | Cancelled Post Market |
| 02299445 | OCTREOTIDE INJECTION | TEVA CANADA LIMITED | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 200 MCG | Cancelled Post Market |
| 02299453 | OCTREOTIDE INJECTION | TEVA CANADA LIMITED | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 500 MCG | Cancelled Post Market |
| 02299429 | OCTREOTIDE INJECTION | TEVA CANADA LIMITED | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 50 MCG | Cancelled Post Market |
| 02299437 | OCTREOTIDE INJECTION | TEVA CANADA LIMITED | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 100 MCG | Cancelled Post Market |
| 02049392 | SANDOSTATIN | NOVARTIS PHARMACEUTICALS CANADA INC | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 200 MCG | Cancelled Post Market |
| 00839213 | SANDOSTATIN | NOVARTIS PHARMACEUTICALS CANADA INC | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 500 MCG | Cancelled Post Market |
| 00839205 | SANDOSTATIN | NOVARTIS PHARMACEUTICALS CANADA INC | Solution | OCTREOTIDE (OCTREOTIDE ACETATE) 100 MCG | Cancelled Post Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 6172 | 2005-01-12 | New Drug Submission (NDS) | NEW MANUFACTURER AND PRODUCT NAME |