APO-GRANISETRON DIN 02308894
Status: Marketed
Holder: APOTEX INC
Molecule: GRANISETRON (GRANISETRON HYDROCHLORIDE)
Available to quote
Health Canada record
| Active ingredient(s) | GRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MG |
|---|---|
| Dosage form | Tablet |
| Route | Oral |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | A04AA02 GRANISETRON |
| Original market date | 20-Feb-2009 |
| Current status date | 16-Sep-2016 |
| Source | Health Canada DPD |
Establishment licence of the holder
Apotex Inc — licence 100375, currently licensed, last inspection rating C (2026-04-21).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing GRANISETRON (GRANISETRON HYDROCHLORIDE)
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02322765 | GRANISETRON HYDROCHLORIDE INJECTION | OMEGA LABORATORIES LIMITED | Liquid | GRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MG | Marketed |
| 02384108 | GRANISETRON HYDROCHLORIDE INJECTION | STRIDES PHARMA CANADA INC | Solution | GRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MG | Approved |
| 02558408 | GRANISETRON HYDROCHLORIDE INJECTION USP | HIKMA CANADA LIMITED | Solution | GRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MG | Approved |
| 02452359 | NAT-GRANISETRON | NATCO PHARMA (CANADA) INC | Tablet | GRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MG | Marketed |
| 02304708 | GRANISETRON HYDROCHLORIDE INJECTION | SANDOZ CANADA INCORPORATED | Liquid | GRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MG | Cancelled Post Market |
| 02385414 | GRANISETRON HYDROCHLORIDE INJECTION SDZ | SANDOZ CANADA INCORPORATED | Solution | GRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MG | Cancelled Post Market |
| 02472686 | JAMP GRANISETRON | JAMP PHARMA CORPORATION | Tablet | GRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MG | Dormant |
| 02088371 | KYTRIL 1MG/1ML | HOFFMANN-LA ROCHE LIMITED | Liquid | GRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MG | Cancelled Post Market |
| 02185881 | KYTRIL TABLETS 1MG | HOFFMANN-LA ROCHE LIMITED | Tablet | GRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MG | Cancelled Post Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 18243 | 2016-07-08 | Abbreviated New Drug Submission (ANDS) | Updates to the Labels Administrative - Transfer of Drug Identification Number |
| 11618 | 2010-07-26 | Abbreviated New Drug Submission (ANDS) | Manufacturer and product name change |
| 10042 | 2009-02-19 | Abbreviated New Drug Submission (ANDS) |