SODIUM EDECRIN DIN 00268313
Status: Dormant
Holder: BAUSCH HEALTH, CANADA INC.
Molecule: ETHACRYNIC ACID (ETHACRYNATE SODIUM)
Available to quote
Health Canada record
| Active ingredient(s) | ETHACRYNIC ACID (ETHACRYNATE SODIUM) 50 MG |
|---|---|
| Dosage form | Powder For Solution |
| Route | Intravenous |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | C03CC01 ETACRYNIC ACID |
| Original market date | 31-Dec-1968 |
| Current status date | 22-Dec-2020 |
| Source | Health Canada DPD |
Establishment licence of the holder
Bausch Health Companies Inc. — licence 101880, currently licensed, last inspection rating C (2026-06-01).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing ETHACRYNIC ACID (ETHACRYNATE SODIUM)
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02462362 | ETHACRYNATE SODIUM | STERIMAX INC | Powder For Solution | ETHACRYNIC ACID (ETHACRYNATE SODIUM) 50 MG | Marketed |
| 02479591 | ETHACRYNATE SODIUM FOR INJECTION | ENDO PAR INNOVATION COMPANY, LLC | Powder For Solution | ETHACRYNIC ACID (ETHACRYNATE SODIUM) 50 MG | Cancelled Pre Market |
| 02469456 | ETHACRYNATE SODIUM FOR INJECTION USP | STERIMAX INC | Powder For Solution | ETHACRYNIC ACID (ETHACRYNATE SODIUM) 50 MG | Dormant |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 24871 | 2020-12-22 | New Drug Submission (NDS) | CHANGE IN PRODUCT OWNERSHIP |
| 13143 | 2012-03-26 | New Drug Submission (NDS) | Manufacturer name change |
| 9131 | 2007-07-25 | New Drug Submission (NDS) | MANUFACTURER NAME CHANGE |