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DEXTROAMPHETAMINE DIN 02443236

Status: Marketed
Holder: AA PHARMA INC
Molecule: DEXTROAMPHETAMINE SULFATE
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Health Canada record

Active ingredient(s)DEXTROAMPHETAMINE SULFATE 5 MG
Dosage formTablet
RouteOral
ScheduleCONTROLLED DRUGS (CDSA I)
ClassHuman
ATCN06BA02 DEXAMFETAMINE
Original market date28-Aug-2015
Current status date31-Oct-2018
SourceHealth Canada DPD

Establishment licence of the holder

AA Pharma Inc. — licence 101851, currently licensed, last inspection rating C (2023-05-23).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing DEXTROAMPHETAMINE SULFATE

DINProductCompanyFormStrengthStatus
02481464APO-DEXTROAMPHETAMINE SRAPOTEX INCCapsule (Sustained-Release)DEXTROAMPHETAMINE SULFATE 10 MGApproved
02481472APO-DEXTROAMPHETAMINE SRAPOTEX INCCapsule (Sustained-Release)DEXTROAMPHETAMINE SULFATE 15 MGApproved
01924516DEXEDRINEKNIGHT THERAPEUTICS INC.TabletDEXTROAMPHETAMINE SULFATE 5 MGMarketed
01924559DEXEDRINE SPANSULEKNIGHT THERAPEUTICS INC.Capsule (Sustained-Release)DEXTROAMPHETAMINE SULFATE 10 MGMarketed
01924567DEXEDRINE SPANSULEKNIGHT THERAPEUTICS INC.Capsule (Sustained-Release)DEXTROAMPHETAMINE SULFATE 15 MGMarketed
02566605PMS-DEXTROAMPHETAMINEPHARMASCIENCE INCTabletDEXTROAMPHETAMINE SULFATE 5 MGApproved
02448327TEVA-DEXTROAMPHETAMINE SRTEVA CANADA LIMITEDCapsule (Sustained-Release)DEXTROAMPHETAMINE SULFATE 15 MGMarketed
02448319TEVA-DEXTROAMPHETAMINE SRTEVA CANADA LIMITEDCapsule (Sustained-Release)DEXTROAMPHETAMINE SULFATE 10 MGMarketed
02447673PMS-DEXTROAMPHETAMINEPHARMASCIENCE INCTabletDEXTROAMPHETAMINE SULFATE 5 MGCancelled Pre Market

Notices of Compliance

NOCDateSubmissionReason
206922018-04-04New Drug Submission (NDS)Change in Product Ownership Revisions to the product monograph and labels
170442015-06-30New Drug Submission (NDS)

International API supply for DEXTROAMPHETAMINE SULFATE

8 active FDA Drug Master Files.

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