99MTC SULPHIDE COLLOID KIT DIN 02354691
Status: Cancelled Pre Market
Holder: ISOLOGIC INNOVATIVE RADIOPHARMACEUTICALS LTD.
Molecule: SODIUM THIOSULFATE
Health Canada record
| Active ingredient(s) | SODIUM THIOSULFATE 3 MG; GELATIN 4 MG; POTASSIUM PERRHENATE 0.5 MG |
|---|---|
| Dosage form | Kit; Solution |
| Route | Subcutaneous; Intradermal; Intravenous |
| Schedule | SCHEDULE C |
| Class | Radiopharmaceutical |
| ATC | |
| Original market date | |
| Current status date | 13-Jun-2022 |
| Source | Health Canada DPD |
Establishment licence of the holder
Isologic Innovative Radiopharmaceuticals of Ontario Limited — licence 102120, currently licensed, last inspection rating I (2026-08-25).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing SODIUM THIOSULFATE
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02386666 | SEACALPHYX | SEAFORD PHARMACEUTICALS INC | Solution | SODIUM THIOSULFATE 250 MG | Marketed |
| 02137186 | SODIUM THIOSULFATE INJECTION USP | PFIZER CANADA ULC | Solution | SODIUM THIOSULFATE 250 MG | Marketed |
| 02428393 | SODIUM THIOSULFATE INJECTION USP | HOPE PHARMACEUTICALS LTD | Solution | SODIUM THIOSULFATE 250 MG | Marketed |
| 02486067 | SULFUR COLLOID KIT | CALGARY RADIOPHARMACEUTICAL CENTRE / ALBERTA HEALTH SERVICES | Solution; Kit | SODIUM THIOSULFATE 80 MG | Marketed |
| 02328933 | TECHNETIUM TC 99M TSC | GE HEALTHCARE CANADA INC | Powder For Solution; Kit; Solution | SODIUM THIOSULFATE 2 MG | Marketed |
| 00713104 | SCARLET PWR | LANGFORD | Powder | SODIUM THIOSULFATE 10 %; MAGNESIUM SULFATE 54 %; SODIUM SULFATE 25 %; GENTIANA LUTEA .2 %; GINGER 1.25 %; LINUM USITATISSIMUM .1 %; FENUGREEK .2 %; IRON OXIDE 1 %; MAGNESIUM CARBONATE 5.25 %; CALCIUM PHOSPHATE (TRIBASIC) 1 %; ETHYLENEDIAMINE DIHYDROIODIDE .008 % | Cancelled Post Market |
| 01908820 | SODIUM THIOSULFATE INJ 25% USP | DAVID BULL LABORATORIES (PTY) LTD. | Liquid | SODIUM THIOSULFATE 250 MG | Cancelled Post Market |
| 02240512 | TOXILAX | JAAPHARM CANADA INC. | Powder | SODIUM THIOSULFATE 10 %; MAGNESIUM SULFATE 54 %; SODIUM SULFATE 25 %; GENTIANA LUTEA 0.2 %; GINGER 1.25 %; LINUM USITATISSIMUM 0.1 %; FENUGREEK 0.2 %; IRON OXIDE 1 %; MAGNESIUM CARBONATE 5.25 %; CALCIUM PHOSPHATE (TRIBASIC) 1 %; ETHYLENEDIAMINE DIHYDROIODIDE 0.008 % | Dormant |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 26006 | 2021-06-03 | New Drug Submission (NDS) | CHANGE IN PRODUCT OWNERSHIP. |
International API supply for SODIUM THIOSULFATE
1 valid EDQM Certificates of Suitability from 1 holders. 7 active FDA Drug Master Files.
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