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MANNITOL INJECTION USP DIN 00038016

Status: Marketed
Holder: ICU MEDICAL CANADA INC
Molecule: MANNITOL

Health Canada record

Active ingredient(s)MANNITOL 20 %
Dosage formSolution
RouteIntravenous
ScheduleETHICAL
ClassHuman
ATCB05BC01 MANNITOL
Original market date31-Dec-1963
Current status date05-Mar-2020
SourceHealth Canada DPD

Establishment licence of the holder

ICU Medical Canada Inc. — licence 3-002455, currently licensed, last inspection rating C (2022-08-23).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing MANNITOL

DINProductCompanyFormStrengthStatus
02489562ARIDOLPHARMAXIS EUROPE LIMITEDKit; PowderMANNITOL 20 MG; MANNITOL 40 MG; MANNITOL 5 MG; MANNITOL 10 MGMarketed
00038024MANNITOL INJECTION USPPFIZER CANADA ULCSolutionMANNITOL 25 %Marketed
02243176MANNITOL INJECTION, USPFRESENIUS KABI CANADA LTDSolutionMANNITOL 25 %Marketed
00060410OSMITROL INJECTION 10%BAXTER CORPORATIONSolutionMANNITOL 10 %Marketed
00060437OSMITROL INJECTION 20%BAXTER CORPORATIONSolutionMANNITOL 20 %Marketed
00037990MANNITOL INJ 10% ABBOVACABBOTT LABORATORIES, LIMITEDLiquidMANNITOL 100 MGCancelled Post Market
00243809MANNITOL INJ 25%INTERNATIONAL MEDICATION SYSTEMS LTD.LiquidMANNITOL 250 MGCancelled Post Market
00729183MANNITOL INJ 25%ASTRA PHARMA INC.LiquidMANNITOL 250 MGCancelled Post Market
00037982MANNITOL INJ 5% ABBOVACABBOTT LABORATORIES, LIMITEDLiquidMANNITOL 50 MGCancelled Post Market
01963953RESECTISOL (5% MANNITOL IRRIGATION)B. BRAUN MEDICAL INCLiquidMANNITOL 5 %Cancelled Post Market

International API supply for MANNITOL

1 valid EDQM Certificates of Suitability from 1 holders. 20 active FDA Drug Master Files.

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