TOCTINO DIN 02337649
Health Canada record
| Active ingredient(s) | ALITRETINOIN 30 MG |
|---|---|
| Dosage form | Capsule |
| Route | Oral |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | D11AH04 ALITRETINOIN |
| Original market date | 19-Nov-2010 |
| Current status date | 14-Jul-2023 |
| Source | Health Canada DPD |
Establishment licence of the holder
GlaxoSmithKline Inc. — licence 100630, currently licensed, last inspection rating C (2025-09-15).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing ALITRETINOIN
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02477432 | HANZEMA | DR. REDDY'S LABORATORIES INC | Capsule | ALITRETINOIN 10 MG | Marketed |
| 02477440 | HANZEMA | DR. REDDY'S LABORATORIES INC | Capsule | ALITRETINOIN 30 MG | Marketed |
| 02240328 | PANRETIN | LIGAND PHARMACEUTICALS INC | Gel | ALITRETINOIN 0.1 % | Cancelled (Unreturned Annual) |
| 02337630 | TOCTINO | GLAXOSMITHKLINE INC | Capsule | ALITRETINOIN 10 MG | Cancelled Post Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 14100 | 2013-02-14 | New Drug Submission (NDS) | Manufacturer name change |
| 11828 | 2010-11-02 | New Drug Submission (NDS) | Manufacturer name change |
| 10780 | 2009-11-13 | New Drug Submission (NDS) |
International API supply for ALITRETINOIN
2 active FDA Drug Master Files.
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