ETHACRYNATE SODIUM FOR INJECTION USP DIN 02469456
Status: Dormant
Holder: STERIMAX INC
Available to quote
Health Canada record
| Active ingredient(s) | ETHACRYNIC ACID (ETHACRYNATE SODIUM) 50 MG |
|---|
| Dosage form | Powder For Solution |
|---|
| Route | Intravenous |
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| Schedule | PRESCRIPTION |
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| Class | Human |
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| ATC | C03CC01 ETACRYNIC ACID |
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| Original market date | 29-Mar-2018 |
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| Current status date | 27-Jun-2024 |
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| Source | Health Canada DPD |
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Establishment licence of the holder
Sterimax Inc — licence 100925, currently licensed, last inspection rating C (2024-05-13).
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 |
| 00268313 | SODIUM EDECRIN | BAUSCH HEALTH, CANADA INC. | Powder For Solution | ETHACRYNIC ACID (ETHACRYNATE SODIUM) 50 MG | Dormant |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|
| 19993 | 2017-11-02 | Abbreviated New Drug Submission (ANDS) | |
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