SOLU-DELTA-CORTEF DIN 01990578
Health Canada record
| Active ingredient(s) | PREDNISOLONE (PREDNISOLONE 21-SUCCINATE SODIUM) 100 MG |
|---|---|
| Dosage form | Powder For Solution |
| Route | Intramuscular; Intravenous |
| Schedule | NON-PRESCRIPTION DRUGS |
| Class | Veterinary |
| ATC | |
| Original market date | 31-Dec-1993 |
| Current status date | 20-Jul-2018 |
| Source | Health Canada DPD |
Establishment licence of the holder
Zoetis Canada Inc — licence 102076, currently licensed, last inspection rating C (2023-10-05).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing PREDNISOLONE (PREDNISOLONE 21-SUCCINATE SODIUM)
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 00553506 | PREDNISOLONE SOD SUCCINATE INJ 10MG/ML | UNIVET PHARMACEUTICALS LTD. | Liquid | PREDNISOLONE (PREDNISOLONE 21-SUCCINATE SODIUM) 10 MG | Cancelled Post Market |
| 01990969 | SOLU-DELTA-CORTEF STERILE SOLUTION | PHARMACIA ANIMAL HEALTH | Powder For Solution | PREDNISOLONE (PREDNISOLONE 21-SUCCINATE SODIUM) 500 MG | Cancelled Post Market |