TULINOVET DIN 02530155
Status: Marketed
Holder: MODERN VETERINARY THERAPEUTICS LLC
Health Canada record
| Active ingredient(s) | TULATHROMYCIN 100 MG |
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| Dosage form | Solution |
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| Route | Intramuscular; Subcutaneous |
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| Schedule | PRESCRIPTION |
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| Class | Veterinary |
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| ATC | |
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| Original market date | 20-Sep-2023 |
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| Current status date | 20-Sep-2023 |
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| Source | Health Canada DPD |
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Establishment licence of the holder
Modern Veterinary Therapeutics Inc — licence 3-002686, currently licensed, last inspection rating I (2026-07-08).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing TULATHROMYCIN
| DIN | Product | Company | Form | Strength | Status |
|---|
| 02532859 | AROVYN | INTERVET CANADA CORP | Solution | TULATHROMYCIN 100 MG | Approved |
| 02285452 | DRAXXIN | ZOETIS CANADA INC | Solution | TULATHROMYCIN 100 MG | Marketed |
| 02430711 | DRAXXIN 25 | ZOETIS CANADA INC | Solution | TULATHROMYCIN 25 MG | Marketed |
| 02516683 | DRAXXIN KP | ZOETIS CANADA INC | Solution | TULATHROMYCIN 100 MG; KETOPROFEN 120 MG | Marketed |
| 02516500 | INCREXXA | ELANCO CANADA LIMITED | Solution | TULATHROMYCIN 100 MG | Marketed |
| 02508990 | LYDAXX | VETOQUINOL N A INC | Solution | TULATHROMYCIN 100 MG | Marketed |
| 02544229 | MACROSYN | BIMEDA-MTC ANIMAL HEALTH INC | Solution | TULATHROMYCIN 100 MG | Marketed |
| 02536013 | TULAJECT | ALIVIRA ANIMAL HEALTH LIMITED | Solution | TULATHROMYCIN 100 MG | Approved |
| 02502151 | TULAVEN | CEVA ANIMAL HEALTH INC | Solution | TULATHROMYCIN 100 MG | Marketed |
| 02502879 | TULISSIN | VIRBAC AH, INC. | Solution | TULATHROMYCIN 100 MG | Marketed |
| 02536277 | TULISSIN 25 | VIRBAC AH, INC. | Solution | TULATHROMYCIN 25 MG | Approved |
| 02560348 | VACASAN | PARNELL TECHNOLOGIES PTY LTD | Solution | TULATHROMYCIN 100 MG | Approved |
| 02518236 | REXXOLIDE | DECHRA REGULATORY BV | Solution | TULATHROMYCIN 100 MG | Dormant |
| 02505401 | TULIEVE | NORBROOK LABORATORIES LTD. | Solution | TULATHROMYCIN 100 MG | Dormant |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|
| 30081 | 2023-02-07 | Supplement to an Abbreviated New Drug Submission (SANDS) | PRODUCT NAME CHANGE |
| 28822 | 2022-08-26 | Abbreviated New Drug Submission (ANDS) | |
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