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MODURET DIN 00487813

Status: Cancelled Post Market
Holder: PREMPHARM INC
Molecule: AMILORIDE HYDROCHLORIDE

Health Canada record

Active ingredient(s)AMILORIDE HYDROCHLORIDE 5 MG; HYDROCHLOROTHIAZIDE 50 MG
Dosage formTablet
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCC03EA01 HYDROCHLOROTHIAZIDE AND POTASSIUM-SPARING AGENTS
Original market date31-Dec-1981
Current status date05-Aug-2009
SourceHealth Canada DPD

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing AMILORIDE HYDROCHLORIDE

DINProductCompanyFormStrengthStatus
02249510MIDAMORAA PHARMA INCTabletAMILORIDE HYDROCHLORIDE 5.0 MGMarketed
00870943AMI-HYDRO TABPRO DOC LIMITEETabletAMILORIDE HYDROCHLORIDE 5 MG; HYDROCHLOROTHIAZIDE 50 MGCancelled Post Market
02257394AMILORIDE HYDROCHLORIDE TABLETS, USPORBUS PHARMA INCTabletAMILORIDE HYDROCHLORIDE 5 MGCancelled (Unreturned Annual)
00487805MIDAMOR TABLETS 5MGORBUS PHARMA INCTabletAMILORIDE HYDROCHLORIDE 5 MGCancelled Post Market
02257378MYLAN-AMILAZIDEMYLAN PHARMACEUTICALS ULCTabletAMILORIDE HYDROCHLORIDE 5 MG; HYDROCHLOROTHIAZIDE 50 MGCancelled Post Market
01937219NOVAMILORTEVA CANADA LIMITEDTabletAMILORIDE HYDROCHLORIDE 5 MG; HYDROCHLOROTHIAZIDE 50 MGCancelled Post Market
02231254PENTA-AMILORIDE HCTZ TABLETSPENTAPHARM LTD.TabletAMILORIDE HYDROCHLORIDE 5 MG; HYDROCHLOROTHIAZIDE 50 MGCancelled (Unreturned Annual)
02242092RIVA-AMILZIDE 5/50 MGLABORATOIRE RIVA INC.TabletAMILORIDE HYDROCHLORIDE 5 MG; HYDROCHLOROTHIAZIDE 50 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
63962005-04-08New Drug Submission (NDS)MANUFACTURER NAME CHANGE
47712004-06-21New Drug Submission (NDS)MANUFACTURER NAME CHANGE

International API supply for AMILORIDE HYDROCHLORIDE

1 active FDA Drug Master Files.

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