KEXXTONE DIN 02451999
Status: Marketed
Holder: ELANCO CANADA LIMITED
Health Canada record
| Active ingredient(s) | MONENSIN (MONENSIN SODIUM) 32.4 G |
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| Dosage form | Capsule |
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| Route | Oral |
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| Schedule | NON-PRESCRIPTION DRUGS |
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| Class | Veterinary |
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| ATC | |
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| Original market date | 05-Jan-2017 |
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| Current status date | 19-Jun-2018 |
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| Source | Health Canada DPD |
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Establishment licence of the holder
Elanco Canada Limited — licence 102236, currently licensed, last inspection rating C (2022-08-03).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing MONENSIN (MONENSIN SODIUM)
| DIN | Product | Company | Form | Strength | Status |
|---|
| 02231172 | COBAN PREMIX | ELANCO CANADA LIMITED | Drug Premix | MONENSIN (MONENSIN SODIUM) 200 G | Marketed |
| 02243232 | MONENSIN PREMIX | BIO AGRI MIX LP | Drug Premix | MONENSIN (MONENSIN SODIUM) 200 G | Marketed |
| 02516772 | MONOVET | HUVEPHARMA EOOD | Drug Premix | MONENSIN (MONENSIN SODIUM) 200 G | Marketed |
| 02231173 | RUMENSIN PREMIX | ELANCO CANADA LIMITED | Drug Premix | MONENSIN (MONENSIN SODIUM) 200 G | Marketed |
| 02082128 | RUMENSIN CRC | ELANCO CANADA LIMITED | Capsule (Extended-Release) | MONENSIN (MONENSIN SODIUM) 32 G | Cancelled Post Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|
| 20077 | 2017-11-21 | New Drug Submission (NDS) | MERGER - BUYOUT |
| 17769 | 2016-02-12 | New Drug Submission (NDS) | |
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