NUMORPHAN SUPPOSITORY 5MG DIN 01916513
Health Canada record
| Active ingredient(s) | OXYMORPHONE HYDROCHLORIDE 5 MG |
|---|---|
| Dosage form | Suppository |
| Route | Rectal |
| Schedule | NARCOTICS (CDSA I) |
| Class | Human |
| ATC | N02AA NATURAL OPIUM ALKALOIDS |
| Original market date | 31-Dec-1993 |
| Current status date | 04-Jul-2002 |
| Source | Health Canada DPD |
Establishment licence of the holder
Bristol-Myers Squibb Canada — licence 100100, currently licensed, last inspection rating C (2026-03-18).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing OXYMORPHONE HYDROCHLORIDE
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 01916505 | NUMORPHAN INJECTION 1.5MG/ML | BRISTOL-MYERS SQUIBB CANADA | Liquid | OXYMORPHONE HYDROCHLORIDE 1.5 MG | Cancelled Post Market |
| 02383403 | OPANA ER | PALADIN PHARMA INC. | Tablet (Extended-Release) | OXYMORPHONE HYDROCHLORIDE 5 MG | Cancelled Pre Market |
| 02383438 | OPANA ER | PALADIN PHARMA INC. | Tablet (Extended-Release) | OXYMORPHONE HYDROCHLORIDE 10 MG | Cancelled Pre Market |
| 02383454 | OPANA ER | PALADIN PHARMA INC. | Tablet (Extended-Release) | OXYMORPHONE HYDROCHLORIDE 20 MG | Cancelled Pre Market |
| 02383470 | OPANA ER | PALADIN PHARMA INC. | Tablet (Extended-Release) | OXYMORPHONE HYDROCHLORIDE 40 MG | Cancelled Pre Market |
International API supply for OXYMORPHONE HYDROCHLORIDE
2 active FDA Drug Master Files.
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