BLEOMYCIN FOR INJECTION USP DIN 02367351
Status: Cancelled Pre Market
Holder: SANDOZ CANADA INCORPORATED
Molecule: BLEOMYCIN (BLEOMYCIN SULFATE)
Health Canada record
| Active ingredient(s) | BLEOMYCIN (BLEOMYCIN SULFATE) 15 UNIT |
|---|---|
| Dosage form | Powder For Solution |
| Route | Intravenous; Intrapleural; Intramuscular; Subcutaneous |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | L01DC01 BLEOMYCIN |
| 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 BLEOMYCIN (BLEOMYCIN SULFATE)
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02265982 | BLEOMYCIN FOR INJECTION | FRESENIUS KABI CANADA LTD | Powder For Solution | BLEOMYCIN (BLEOMYCIN SULFATE) 15 UNIT | Marketed |
| 02566346 | BLEOMYCIN FOR INJECTION | MARCAN PHARMACEUTICALS INC | Powder For Solution | BLEOMYCIN (BLEOMYCIN SULFATE) 15 UNIT | Approved |
| 02131692 | BLEOMYCIN FOR INJECTION USP | PFIZER CANADA ULC | Powder For Solution | BLEOMYCIN (BLEOMYCIN SULFATE) 15 UNIT | Marketed |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 12293 | 2011-04-27 | Abbreviated New Drug Submission (ANDS) |