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RISEDRONATE DIN 02370247

Status: Cancelled Pre Market
Holder: SANIS HEALTH INC
Molecule: RISEDRONATE SODIUM (RISEDRONATE SODIUM MONOHYDRATE)

Health Canada record

Active ingredient(s)RISEDRONATE SODIUM (RISEDRONATE SODIUM MONOHYDRATE) 30 MG
Dosage formTablet
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCM05BA07 RISEDRONIC ACID
Original market date
Current status date24-Jan-2019
SourceHealth Canada DPD

Establishment licence of the holder

Sanis Health Inc. — licence 101796, currently licensed, last inspection rating I (2024-07-23).

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
02358891NTP-RISEDRONATENT PHARMA CANADA LTDTabletRISEDRONATE SODIUM (RISEDRONATE SODIUM MONOHYDRATE) 30 MGCancelled Pre Market
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
02370239RISEDRONATESANIS HEALTH INCTabletRISEDRONATE SODIUM (RISEDRONATE SODIUM MONOHYDRATE) 5 MGCancelled Pre Market
02326981TEVA-RISEDRONATE/CALCIUMTEVA CANADA LIMITEDTablet; KitRISEDRONATE SODIUM (RISEDRONATE SODIUM MONOHYDRATE) 35 MG; CALCIUM (CALCIUM CARBONATE) 500 MGCancelled Pre Market

Notices of Compliance

NOCDateSubmissionReason
155232014-04-23Abbreviated New Drug Submission (ANDS)LICENSING AGREEMENT BETWEEN TWO COMPANIES
126502011-09-22Abbreviated New Drug Submission (ANDS)New Manufacturer and Product Name
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