Kétoprofène in Canada
47 medicine records from 17 holders carry this name in the official sources. Collected on November 10, 2026.
Medicines
| Name | Holder | Status | Code |
|---|---|---|---|
| ANAFEN · 100 MG per ML · SOLUTION | BOEHRINGER INGELHEIM ANIMAL HEALTH CANADA INC. | cancelled |
DIN
01938126DPD drug code
13635
|
| ANAFEN INJECTION 10MG/ML · 10 MG per ML · SOLUTION | MERIAL CANADA INC | cancelled |
DIN
02150999DPD drug code
18303
|
| ANAFEN TABLETS 10MG/TAB · 10 MG · TABLET | MERIAL CANADA INC | cancelled |
DIN
02150972DPD drug code
18300
|
| ANAFEN TABLETS 20MG/TAB · 20 MG · TABLET | MERIAL CANADA INC | cancelled |
DIN
02150980DPD drug code
18302
|
| ANAFEN TABLETS 5MG/TAB · 5 MG · TABLET | MERIAL CANADA INC | cancelled |
DIN
02150964DPD drug code
18301
|
| DRAXXIN KP · 120 MG per ML + 100 MG per ML · SOLUTION | ZOETIS CANADA INC | authorised |
DIN
02516683DPD drug code
100602
|
| FARMAFEN · 100 MG per ML · SOLUTION | BIMEDA-MTC ANIMAL HEALTH INC | authorised |
DIN
02534606DPD drug code
102351
|
| KETOPROFEN · 50 MG · CAPSULE | AA PHARMA INC | authorised |
DIN
00790427DPD drug code
10136
|
| KETOPROFEN-E · 100 MG · TABLET (ENTERIC-COATED) | AA PHARMA INC | authorised |
DIN
00842664DPD drug code
10134
|
| KETOPROFEN-E · 50 MG · TABLET (ENTERIC-COATED) | AA PHARMA INC | authorised |
DIN
00790435DPD drug code
10135
|
| KETOPROFEN-E ECT 100MG · 100 MG per ECT · TABLET (ENTERIC-COATED) | PRO DOC LIMITEE | cancelled |
DIN
02084198DPD drug code
20110
|
| KETOPROFEN-E ECT 50MG · 50 MG per ECT · TABLET (ENTERIC-COATED) | PRO DOC LIMITEE | cancelled |
DIN
02084171DPD drug code
19206
|
| KETOPROFEN SR · 200 MG · TABLET (EXTENDED-RELEASE) | AA PHARMA INC | authorised |
DIN
02172577DPD drug code
19115
|
| KETOPROFEN-SR - SRT 200MG · 200 MG per TAB · TABLET (EXTENDED-RELEASE) | PRO DOC LIMITEE | cancelled |
DIN
02210487DPD drug code
43046
|
| KETOPROFEN SUPPOSITORIES · 100 MG · SUPPOSITORY | PHARMEL INC | cancelled |
DIN
02237011DPD drug code
60312
|
| KETOPROFEN SUPPOSITORIES · 50 MG per SUP · SUPPOSITORY | PHARMEL INC | cancelled |
DIN
02236965DPD drug code
60260
|
| KETOPROFEN V · 100 MG per ML · SOLUTION | MODERN VETERINARY THERAPEUTICS LLC | authorised |
DIN
02446316DPD drug code
93165
|
| NOVO-KETO-EC TAB 100MG · 100 MG per TAB · TABLET (ENTERIC-COATED) | NOVOPHARM LIMITED | cancelled |
DIN
01981536DPD drug code
12958
|
| NOVO-KETO-EC TAB 50MG · 50 MG per TAB · TABLET (ENTERIC-COATED) | NOVOPHARM LIMITED | cancelled |
DIN
01981528DPD drug code
12957
|
| NOVO-KETO SUPPOSITORIES 100MG · 100 MG per SUP · SUPPOSITORY | NOVOPHARM LIMITED | cancelled |
DIN
02156083DPD drug code
20152
|
| NU-KETOPROFEN CAP 50MG · 50 MG · CAPSULE | NU-PHARM INC | cancelled |
DIN
02044633DPD drug code
16039
|
| NU-KETOPROFEN-E ECT 100MG · 100 MG per ECT · TABLET (ENTERIC-COATED) | NU-PHARM INC | cancelled |
DIN
02044641DPD drug code
16038
|
| NU-KETOPROFEN-E ECT 50MG · 50 MG per ECT · TABLET (ENTERIC-COATED) | NU-PHARM INC | cancelled |
DIN
02044781DPD drug code
16042
|
| ORAFEN - SUP RT 100MG · 100 MG per SUP · SUPPOSITORY | TECHNILAB PHARMA INC. | cancelled |
DIN
02165481DPD drug code
19796
|
| ORUDIS 100 · 100 MG · SUPPOSITORY | AVENTIS PHARMA INC | cancelled |
DIN
01926411DPD drug code
12752
|
| ORUDIS 50 · 50 MG · SUPPOSITORY | AVENTIS PHARMA INC | cancelled |
DIN
01931512DPD drug code
11976
|
| ORUDIS CAP 50MG · 50 MG · CAPSULE | AVENTIS PHARMA INC | cancelled |
DIN
01926403DPD drug code
12543
|
| ORUDIS E-100 · 100 MG · TABLET (ENTERIC-COATED) | AVENTIS PHARMA INC | cancelled |
DIN
01926365DPD drug code
11971
|
| ORUDIS E-50 · 50 MG · TABLET (ENTERIC-COATED) | AVENTIS PHARMA INC | cancelled |
DIN
01926381DPD drug code
12652
|
| ORUDIS SR-200 · 200 MG · TABLET (EXTENDED-RELEASE) | AVENTIS PHARMA INC | cancelled |
DIN
01926373DPD drug code
12836
|
| ORUVAIL 150 · 150 MG per CAP · CAPSULE (SUSTAINED-RELEASE) | AVENTIS PHARMA INC | cancelled |
DIN
01913050DPD drug code
11318
|
| ORUVAIL 200 · 200 MG per CAP · CAPSULE (SUSTAINED-RELEASE) | AVENTIS PHARMA INC | cancelled |
DIN
01913069DPD drug code
11319
|
| PMS-KETOPROFEN · 100 MG · SUPPOSITORY | PHARMASCIENCE INC | cancelled |
DIN
02015951DPD drug code
14025
|
| PMS-KETOPROFEN · 50 MG · SUPPOSITORY | PHARMASCIENCE INC | cancelled |
DIN
02148773DPD drug code
19507
|
| PMS-KETOPROFEN CAPSULES · 50 MG · CAPSULE | PHARMASCIENCE INC | cancelled |
DIN
02150808DPD drug code
19340
|
| PMS-KETOPROFEN E-100 - ECT · 100 MG per ECT · TABLET (ENTERIC-COATED) | PHARMASCIENCE INC | cancelled |
DIN
02150824DPD drug code
19338
|
| PMS-KETOPROFEN E-50 - ECT 50MG · 50 MG per ECT · TABLET (ENTERIC-COATED) | PHARMASCIENCE INC | cancelled |
DIN
02150816DPD drug code
19339
|
| RHODIS · 100 MG per SUP · SUPPOSITORY | SANOFI-AVENTIS CANADA INC | cancelled |
DIN
00761699DPD drug code
8928
|
| RHODIS CAP 50MG · 50 MG per CAP · CAPSULE | RHODIAPHARM INC | cancelled |
DIN
00761664DPD drug code
8623
|
| RHODIS EC · 100 MG · TABLET (ENTERIC-COATED) | SANOFI-AVENTIS CANADA INC | cancelled |
DIN
00761680DPD drug code
8625
|
| RHODIS EC · 50 MG · TABLET (ENTERIC-COATED) | SANOFI-AVENTIS CANADA INC | cancelled |
DIN
00761672DPD drug code
8624
|
| RHODIS SR 200MG · 200 MG per SRT · TABLET (EXTENDED-RELEASE) | RHODIAPHARM INC | cancelled |
DIN
02031175DPD drug code
18728
|
| RHOVAIL 150 · 150 MG · CAPSULE (SUSTAINED-RELEASE) | RHODIAPHARM INC | cancelled |
DIN
02183099DPD drug code
19427
|
| RHOVAIL 200 · 200 MG · CAPSULE (SUSTAINED-RELEASE) | RHODIAPHARM INC | cancelled |
DIN
02183102DPD drug code
19426
|
| RIFEN · 100 MG per ML · SOLUTION | VETVIVA RICHTER GMBH | authorised |
DIN
02519801DPD drug code
100903
|
| TEVA-KETOPROFEN · 20 MG · TABLET | TEVA CANADA LIMITED | cancelled |
DIN
02245967DPD drug code
70093
|
| TEVA-KETOPROFEN · 5 MG · TABLET | TEVA CANADA LIMITED | cancelled |
DIN
02245966DPD drug code
70092
|
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