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QUINIDINE SULFATE INJECTION 190MG/ML DIN 00497525

Status: Cancelled Post Market
Holder: HOSPIRA HEALTHCARE ULC
Molecule: QUINIDINE SULFATE

Health Canada record

Active ingredient(s)QUINIDINE SULFATE 190 MG
Dosage formSolution
RouteIntramuscular
ScheduleETHICAL
ClassHuman
ATCC01BA01 QUINIDINE
Original market date31-Dec-1981
Current status date10-Sep-2018
SourceHealth Canada DPD

Establishment licence of the holder

Hospira Healthcare India Pvt. Ltd. — licence , not currently licensed, last inspection rating NC (2017-07-10).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing QUINIDINE SULFATE

DINProductCompanyFormStrengthStatus
00441740APO QUINIDINE TAB 200MGAPOTEX INCTabletQUINIDINE SULFATE 200 MGCancelled Post Market
00021733NOVO-QUINIDIN 200MGNOVOPHARM LIMITEDTabletQUINIDINE SULFATE 200 MGCancelled Post Market
02043505QUINIDEX EXTENTABS SRT 300MGWYETH-AYERST CANADA INC.Tablet (Extended-Release)QUINIDINE SULFATE 300 MGCancelled Post Market
01913883QUINIDEX EXTENTABS SRT 300MGAYERST LABORATORIESTablet (Extended-Release)QUINIDINE SULFATE 300 MGCancelled Post Market
00563692QUINIDINE 200 TABPRO DOC LIMITEETabletQUINIDINE SULFATE 200 MGCancelled Post Market
00026883QUINIDINE SULFATE 200MGROUGIER PHARMA DIVISION OF RATIOPHARM INCTabletQUINIDINE SULFATE 200 MGCancelled Post Market
00004782QUINIDINE SULFATE TAB 200MGGLAXO WELLCOME INC.TabletQUINIDINE SULFATE 200 MGCancelled Post Market
00179256QUINIDINE SULFATE TAB 200MGSTANLEY PHARMACEUTICALS, A DIVISION OF VITA HEALTH PRODUCTS INC.TabletQUINIDINE SULFATE 195 MGCancelled Post Market

International API supply for QUINIDINE SULFATE

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

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