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TEVA-RISEDRONATE/CALCIUM DIN 02326981

Status: Cancelled Pre Market
Holder: TEVA CANADA LIMITED
Molecule: RISEDRONATE SODIUM (RISEDRONATE SODIUM MONOHYDRATE)

Health Canada record

Active ingredient(s)RISEDRONATE SODIUM (RISEDRONATE SODIUM MONOHYDRATE) 35 MG; CALCIUM (CALCIUM CARBONATE) 500 MG
Dosage formTablet; Kit
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCM05BB02 RISEDRONIC ACID AND CALCIUM, SEQUENTIAL
Original market date
Current status date29-Jul-2021
SourceHealth Canada DPD

Establishment licence of the holder

Teva Canada Limited — licence 101810, currently licensed, last inspection rating C (2025-03-04).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing RISEDRONATE SODIUM (RISEDRONATE SODIUM MONOHYDRATE)

DINProductCompanyFormStrengthStatus
02411407RISEDRONATESIVEM PHARMACEUTICALS ULCTabletRISEDRONATE SODIUM (RISEDRONATE SODIUM MONOHYDRATE) 35 MGMarketed
02298384TEVA-RISEDRONATETEVA CANADA LIMITEDTabletRISEDRONATE SODIUM (RISEDRONATE SODIUM MONOHYDRATE) 30 MGMarketed
02298392TEVA-RISEDRONATETEVA CANADA LIMITEDTabletRISEDRONATE SODIUM (RISEDRONATE SODIUM MONOHYDRATE) 35 MGMarketed
02298376TEVA-RISEDRONATETEVA CANADA LIMITEDTabletRISEDRONATE SODIUM (RISEDRONATE SODIUM MONOHYDRATE) 5 MGMarketed
02413809TEVA-RISEDRONATETEVA CANADA LIMITEDTabletRISEDRONATE SODIUM (RISEDRONATE SODIUM MONOHYDRATE) 150 MGMarketed
02358905NTP-RISEDRONATENT PHARMA CANADA LTDTabletRISEDRONATE SODIUM (RISEDRONATE SODIUM MONOHYDRATE) 35 MGCancelled Pre Market
02358883NTP-RISEDRONATENT PHARMA CANADA LTDTabletRISEDRONATE SODIUM (RISEDRONATE SODIUM MONOHYDRATE) 5 MGCancelled Pre Market
02358891NTP-RISEDRONATENT PHARMA CANADA LTDTabletRISEDRONATE SODIUM (RISEDRONATE SODIUM MONOHYDRATE) 30 MGCancelled Pre Market
02370239RISEDRONATESANIS HEALTH INCTabletRISEDRONATE SODIUM (RISEDRONATE SODIUM MONOHYDRATE) 5 MGCancelled Pre Market
02370247RISEDRONATESANIS HEALTH INCTabletRISEDRONATE SODIUM (RISEDRONATE SODIUM MONOHYDRATE) 30 MGCancelled Pre Market

Notices of Compliance

NOCDateSubmissionReason
206852018-03-29Abbreviated New Drug Submission (ANDS)
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