ISOFLURANE USP DIN 02237518
Health Canada record
| Active ingredient(s) | ISOFLURANE 99.9 % |
|---|---|
| Dosage form | Liquid |
| Route | Inhalation |
| Schedule | PRESCRIPTION |
| Class | Veterinary |
| ATC | |
| Original market date | 23-Sep-2009 |
| Current status date | 25-Feb-2015 |
| Source | Health Canada DPD |
Establishment licence of the holder
Fresenius Kabi Canada Ltd. — licence 102232, currently licensed, last inspection rating C (2025-10-01).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing ISOFLURANE
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02225875 | AERRANE | BAXTER CORPORATION | Liquid | ISOFLURANE 100 % | Marketed |
| 02188856 | FORANE | BAXTER CORPORATION | Liquid | ISOFLURANE 100 % | Marketed |
| 02231929 | ISOFLURANE USP | FRESENIUS KABI CANADA LTD | Liquid | ISOFLURANE 99.9 % | Marketed |
| 02091267 | AERRANE | OHMEDA PHARMACEUTICAL PRODUCTS, DIVISION OF BOC CANADA LIMITED | Gas | ISOFLURANE 100 % | Cancelled Post Market |
| 02056666 | FORANE LIQ INH | OHMEDA PHARMACEUTICAL PRODUCTS, DIVISION OF BOC CANADA LIMITED | Liquid | ISOFLURANE 100 % | Cancelled Post Market |
| 02026635 | ISOFLO | ZOETIS CANADA INC | Liquid | ISOFLURANE 99.9 % | Cancelled Post Market |
| 02157217 | ISOFLURANE USP | BIMEDA-MTC ANIMAL HEALTH INC | Liquid | ISOFLURANE 100 % | Dormant |
| 02032384 | ISOFLURANE USP | ABBVIE CORPORATION | Liquid | ISOFLURANE 99.9 % | Cancelled Post Market |
| 02237684 | ISOFLURANE USP | TECHNILAB PHARMA INC. | Liquid | ISOFLURANE 100 % | Cancelled Post Market |
| 02241315 | ISOFLURANE USP | HALOCARBON LABORATORIES, A DIVISION OF HALOCARBON PRODUCTS CORP | Liquid | ISOFLURANE 99.9 % | Cancelled Post Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 16631 | 2015-02-24 | Abbreviated New Drug Submission (ANDS) | MERGER/BUYOUT |
| 6143 | 2002-01-14 | New Drug Submission (NDS) | |
| 6768 | 1998-03-06 | New Drug Submission (NDS) |
International API supply for ISOFLURANE
2 valid EDQM Certificates of Suitability from 2 holders. 5 active FDA Drug Master Files.
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