AXERT 6.25MG DIN 02248128
Status: Cancelled Post Market
Holder: MCNEIL CONSUMER HEALTHCARE DIVISION OF JOHNSON & JOHNSON INC
Molecule: ALMOTRIPTAN (ALMOTRIPTAN MALATE)
Health Canada record
| Active ingredient(s) | ALMOTRIPTAN (ALMOTRIPTAN MALATE) 6.25 MG |
|---|---|
| Dosage form | Tablet |
| Route | Oral |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | N02CC05 ALMOTRIPTAN |
| Original market date | 08-Dec-2003 |
| Current status date | 27-Oct-2017 |
| Source | Health Canada DPD |
Establishment licence of the holder
McNeil Consumer & Specialty Pharmaceuticals — licence , not currently licensed, last inspection rating C (2018-06-12).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing ALMOTRIPTAN (ALMOTRIPTAN MALATE)
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02570297 | AG-ALMOTRIPTAN | ANGITA PHARMA INC. | Tablet | ALMOTRIPTAN (ALMOTRIPTAN MALATE) 12.5 MG | Approved |
| 02570289 | AG-ALMOTRIPTAN | ANGITA PHARMA INC. | Tablet | ALMOTRIPTAN (ALMOTRIPTAN MALATE) 6.25 MG | Approved |
| 02466821 | ALMOTRIPTAN | SANIS HEALTH INC | Tablet | ALMOTRIPTAN (ALMOTRIPTAN MALATE) 12.5 MG | Marketed |
| 02424029 | ALMOTRIPTAN | PRO DOC LIMITEE | Tablet | ALMOTRIPTAN (ALMOTRIPTAN MALATE) 12.5 MG | Marketed |
| 02556022 | JAMP ALMOTRIPTAN | JAMP PHARMA CORPORATION | Tablet | ALMOTRIPTAN (ALMOTRIPTAN MALATE) 6.25 MG | Approved |
| 02556030 | JAMP ALMOTRIPTAN | JAMP PHARMA CORPORATION | Tablet | ALMOTRIPTAN (ALMOTRIPTAN MALATE) 12.5 MG | Approved |
| 02398443 | MYLAN-ALMOTRIPTAN | MYLAN PHARMACEUTICALS ULC | Tablet | ALMOTRIPTAN (ALMOTRIPTAN MALATE) 12.5 MG | Marketed |
| 02398435 | MYLAN-ALMOTRIPTAN | MYLAN PHARMACEUTICALS ULC | Tablet | ALMOTRIPTAN (ALMOTRIPTAN MALATE) 6.25 MG | Marketed |
| 02405334 | SANDOZ ALMOTRIPTAN | SANDOZ CANADA INCORPORATED | Tablet | ALMOTRIPTAN (ALMOTRIPTAN MALATE) 12.5 MG | Marketed |
| 02434849 | TEVA-ALMOTRIPTAN | TEVA CANADA LIMITED | Tablet | ALMOTRIPTAN (ALMOTRIPTAN MALATE) 12.5 MG | Marketed |
| 02405806 | APO-ALMOTRIPTAN | APOTEX INC | Tablet | ALMOTRIPTAN (ALMOTRIPTAN MALATE) 12.5 MG | Dormant |
| 02405792 | APO-ALMOTRIPTAN | APOTEX INC | Tablet | ALMOTRIPTAN (ALMOTRIPTAN MALATE) 6.25 MG | Dormant |
| 02248129 | AXERT 12.5MG | MCNEIL CONSUMER HEALTHCARE DIVISION OF JOHNSON & JOHNSON INC | Tablet | ALMOTRIPTAN (ALMOTRIPTAN MALATE) 12.5 MG | Cancelled Post Market |
| 02441411 | PMS-ALMOTRIPTAN | PHARMASCIENCE INC | Tablet | ALMOTRIPTAN (ALMOTRIPTAN MALATE) 12.5 MG | Cancelled Pre Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 8393 | 2006-11-07 | New Drug Submission (NDS) | MANUFACTURER NAME CHANGE |
| 26 | 2003-09-29 | New Drug Submission (NDS) |