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NOVOLIN GE TORONTO PENFILL DIN 02024284

Status: Cancelled Post Market
Holder: NOVO NORDISK CANADA INC
Molecule: INSULIN INJECTION HUMAN BIOSYNTHETIC
Available to quote

Health Canada record

Active ingredient(s)INSULIN INJECTION HUMAN BIOSYNTHETIC 100 UNIT
Dosage formSolution
RouteIntramuscular; Intravenous; Subcutaneous
ScheduleSCHEDULE D
ClassHuman
ATCA10AB01 INSULIN (HUMAN)
Original market date31-Dec-1993
Current status date20-Mar-2026
SourceHealth Canada DPD

Establishment licence of the holder

Novo Nordisk Canada Inc — licence 100175, currently licensed, last inspection rating C (2023-02-13).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing INSULIN INJECTION HUMAN BIOSYNTHETIC

DINProductCompanyFormStrengthStatus
02466864ENTUZITY KWIKPENELI LILLY CANADA INCSolutionINSULIN INJECTION HUMAN BIOSYNTHETIC 500 UNITMarketed
01959212HUMULIN 30/70 CARTRIDGEELI LILLY CANADA INCSuspensionINSULIN INJECTION HUMAN BIOSYNTHETIC 30 UNIT; INSULIN ISOPHANE HUMAN BIOSYNTHETIC 70 UNITMarketed
01959220HUMULIN R CARTRIDGEELI LILLY CANADA INCSolutionINSULIN INJECTION HUMAN BIOSYNTHETIC 100 UNITMarketed
02024217NOVOLIN GE 30/70NOVO NORDISK CANADA INCSuspensionINSULIN INJECTION HUMAN BIOSYNTHETIC 30 UNIT; INSULIN ISOPHANE HUMAN BIOSYNTHETIC 70 UNITMarketed
02024233NOVOLIN GE TORONTONOVO NORDISK CANADA INCSolutionINSULIN INJECTION HUMAN BIOSYNTHETIC 100 UNITMarketed
01962639HUMULIN 10/90 CARTRIDGEELI LILLY CANADA INCSuspensionINSULIN INJECTION HUMAN BIOSYNTHETIC 10 UNIT; INSULIN ISOPHANE HUMAN BIOSYNTHETIC 90 UNITCancelled Post Market
00889113HUMULIN 10/90 INJELI LILLY CANADA INCSuspensionINSULIN INJECTION HUMAN BIOSYNTHETIC 10 UNIT; INSULIN ISOPHANE HUMAN BIOSYNTHETIC 90 UNITCancelled Post Market
01962655HUMULIN 20/80 CARTRIDGEELI LILLY CANADA INCSuspensionINSULIN INJECTION HUMAN BIOSYNTHETIC 20 UNIT; INSULIN ISOPHANE HUMAN BIOSYNTHETIC 80 UNITCancelled Post Market
00889105HUMULIN 20/80 INJELI LILLY CANADA INCSuspensionINSULIN INJECTION HUMAN BIOSYNTHETIC 20 UNIT; INSULIN ISOPHANE HUMAN BIOSYNTHETIC 80 UNITCancelled Post Market
01962647HUMULIN 40/60 CARTRIDGEELI LILLY CANADA INCSuspensionINSULIN INJECTION HUMAN BIOSYNTHETIC 40 UNIT; INSULIN ISOPHANE HUMAN BIOSYNTHETIC 60 UNITCancelled Post Market
00889091HUMULIN 40/60 INJELI LILLY CANADA INCSuspensionINSULIN INJECTION HUMAN BIOSYNTHETIC 40 UNIT; INSULIN ISOPHANE HUMAN BIOSYNTHETIC 60 UNITCancelled Post Market
01962663HUMULIN 50/50 CARTRIDGEELI LILLY CANADA INCSuspensionINSULIN INJECTION HUMAN BIOSYNTHETIC 50 UNIT; INSULIN ISOPHANE HUMAN BIOSYNTHETIC 50 UNITCancelled Post Market
00889121HUMULIN 50/50 INJELI LILLY CANADA INCSuspensionINSULIN INJECTION HUMAN BIOSYNTHETIC 50 UNIT; INSULIN ISOPHANE HUMAN BIOSYNTHETIC 50 UNITCancelled Post Market
02024292NOVOLIN GE 10/90 PENFILL INJ SUSNOVO NORDISK A/SSuspensionINSULIN INJECTION HUMAN BIOSYNTHETIC 10 UNIT; INSULIN ISOPHANE HUMAN BIOSYNTHETIC 90 UNITCancelled Post Market
02024306NOVOLIN GE 20/80 PENFILL INJ SUSNOVO NORDISK A/SSuspensionINSULIN INJECTION HUMAN BIOSYNTHETIC 20 UNIT; INSULIN ISOPHANE HUMAN BIOSYNTHETIC 80 UNITCancelled Post Market
02025248NOVOLIN GE 30/70 PENFILLNOVO NORDISK CANADA INCSuspensionINSULIN INJECTION HUMAN BIOSYNTHETIC 30 UNIT; INSULIN ISOPHANE HUMAN BIOSYNTHETIC 70 UNITCancelled Post Market
02024314NOVOLIN GE 40/60 PENFILLNOVO NORDISK CANADA INCSuspensionINSULIN INJECTION HUMAN BIOSYNTHETIC 40 UNIT; INSULIN ISOPHANE HUMAN BIOSYNTHETIC 60 UNITCancelled Post Market
02024322NOVOLIN GE 50/50 PENFILLNOVO NORDISK CANADA INCSuspensionINSULIN INJECTION HUMAN BIOSYNTHETIC 50 UNIT; INSULIN ISOPHANE HUMAN BIOSYNTHETIC 50 UNITCancelled Post Market
02024446NOVOLINSET GE 30/70 INJ SUSNOVO NORDISK A/SSuspensionINSULIN INJECTION HUMAN BIOSYNTHETIC 30 UNIT; INSULIN ISOPHANE HUMAN BIOSYNTHETIC 70 UNITCancelled Post Market
02025256NOVOLINSET GE TORONTO INJ LIQ 100U/MLNOVO NORDISK A/SLiquidINSULIN INJECTION HUMAN BIOSYNTHETIC 100 UNITCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
120202011-01-07New Drug Submission (NDS)Manufacturer name change
56821994-07-19Supplement to a New Drug Submission (SNDS)NEW PACKAGE SIZE, REVISED PRODUCT MONOGRAPH
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