AMPHOTEC 50 MG DIN 02241750
Status: Cancelled Post Market
Holder: THREE RIVERS PHARMACEUTICALS LLC
Health Canada record
| Active ingredient(s) | AMPHOTERICIN B 50 MG |
|---|
| Dosage form | Powder For Suspension |
|---|
| Route | Intravenous |
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| Schedule | PRESCRIPTION |
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| Class | Human |
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| ATC | J02AA01 AMPHOTERICIN B |
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| Original market date | 26-Feb-2007 |
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| Current status date | 22-Aug-2013 |
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| Source | Health Canada DPD |
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No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing AMPHOTERICIN B
| DIN | Product | Company | Form | Strength | Status |
|---|
| 02241630 | AMBISOME | ASTELLAS PHARMA CANADA INC | Powder For Solution | AMPHOTERICIN B 50 MG | Marketed |
| 02405032 | AMPHOTERICIN B FOR INJECTION, USP | STERIMAX INC | Powder For Solution | AMPHOTERICIN B 50 MG | Approved |
| 00029149 | FUNGIZONE | CHEPLAPHARM ARZNEIMITTEL GMBH | Powder For Solution | AMPHOTERICIN B 50 MG | Marketed |
| 02554186 | TARO-AMPHOTERICIN B LIPOSOMAL | TARO PHARMACEUTICALS INC | Powder For Solution | AMPHOTERICIN B 50 MG | Approved |
| 02231590 | ABELCET | LEADIANT BIOSCIENCES, INC | Suspension | AMPHOTERICIN B 5 MG | Cancelled Post Market |
| 02241749 | AMPHOTEC 100 MG | THREE RIVERS PHARMACEUTICALS LLC | Powder For Suspension | AMPHOTERICIN B 100 MG | Cancelled Post Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|
| 7704 | 2006-01-26 | New Drug Submission (NDS) | MANUFACTURER NAME CHANGE |
| 76 | 2003-06-11 | New Drug Submission (NDS) | MANUFACTURER NAME CHANGE |
| 963 | 2000-04-26 | New Drug Submission (NDS) | |
International API supply for AMPHOTERICIN B
3 valid EDQM Certificates of Suitability from 3 holders. 6 active FDA Drug Master Files.
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