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APO-VALPROIC ACID ORAL SOLUTION DIN 02238370

Status: Dormant
Holder: APOTEX INC
Molecule: VALPROIC ACID (SODIUM VALPROATE)

Health Canada record

Active ingredient(s)VALPROIC ACID (SODIUM VALPROATE) 250 MG
Dosage formSolution
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCN03AG01 VALPROIC ACID
Original market date15-Jul-1998
Current status date07-Oct-2024
SourceHealth Canada DPD

Establishment licence of the holder

Apotex Inc — licence 100375, currently licensed, last inspection rating C (2026-04-21).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing VALPROIC ACID (SODIUM VALPROATE)

DINProductCompanyFormStrengthStatus
00443832DEPAKENEBGP PHARMA ULCSolutionVALPROIC ACID (SODIUM VALPROATE) 250 MGMarketed
02532441JAMP VALPROIC ACID ORAL SOLUTIONJAMP PHARMA CORPORATIONSolutionVALPROIC ACID (SODIUM VALPROATE) 250 MGMarketed
02549190ODAN-VALPROIC ACIDODAN LABORATORIESLTDSolutionVALPROIC ACID (SODIUM VALPROATE) 250 MGMarketed
02236807PMS-VALPROIC ACIDPHARMASCIENCE INCSolutionVALPROIC ACID (SODIUM VALPROATE) 250 MGMarketed
02238069VALPROIC ACID ORAL SOLUTIONAPOTEX INCSolutionVALPROIC ACID (SODIUM VALPROATE) 250 MGApproved
00443840DEPAKENEBGP PHARMA ULCCapsuleVALPROIC ACID (SODIUM VALPROATE) 250 MGCancelled Post Market
02238042DEPROIC SYRUPTECHNILAB PHARMA INC.SyrupVALPROIC ACID (SODIUM VALPROATE) 250 MGCancelled Post Market
02238817DOM-VALPROIC ACIDDOMINION PHARMACALSolutionVALPROIC ACID (SODIUM VALPROATE) 250 MGCancelled Post Market
02238368EPIJECT I.V.ABBOTT LABORATORIES, LIMITEDLiquidVALPROIC ACID (SODIUM VALPROATE) 500 MGCancelled Post Market
02238210PHL-VALPROIC ACIDPHARMEL INCSyrupVALPROIC ACID (SODIUM VALPROATE) 250 MGCancelled Post Market
02140063RATIO-VALPROIC 50MG/ML SYRUPRATIOPHARM INC DIVISION OF TEVA CANADA LIMITEDSyrupVALPROIC ACID (SODIUM VALPROATE) 50 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
264222021-08-13Abbreviated New Drug Submission (ANDS)Administrative: Product Name Change Administrative: Licensing Agreement Between Two Companies
31621998-07-14Abbreviated New Drug Submission (ANDS)
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