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PRIMIDONE 250 TAB DIN 00563706

Status: Cancelled Post Market
Holder: PRO DOC LIMITEE
Molecule: PRIMIDONE

Health Canada record

Active ingredient(s)PRIMIDONE 250 MG
Dosage formTablet
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCN03AA03 PRIMIDONE
Original market date31-Dec-1982
Current status date12-Aug-1999
SourceHealth Canada DPD

Establishment licence of the holder

Pro Doc Limitée — licence 100182, currently licensed, last inspection rating C (2025-08-11).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing PRIMIDONE

DINProductCompanyFormStrengthStatus
00396761PRIMIDONEAA PHARMA INCTabletPRIMIDONE 250 MGMarketed
00399310PRIMIDONEAA PHARMA INCTabletPRIMIDONE 125 MGMarketed
02042355MYSOLINE 250MG TABELAN PHARMACEUTICALS INCTabletPRIMIDONE 250 MGCancelled Post Market
02042363MYSOLINE PEDIATRIC CHEWABLE TABLETS 125MGELAN PHARMACEUTICALS INCTabletPRIMIDONE 125 MGCancelled Post Market
00002631MYSOLINE PRIMIDONE TABLETS 250MGAYERST VETERINARY LABORATORIESTabletPRIMIDONE 250 MGCancelled Post Market
00002623MYSOLINE TAB 125MGAYERST LABORATORIESTabletPRIMIDONE 125 MGCancelled Post Market
00563714PRIMIDONE 125 TABPRO DOC LIMITEETabletPRIMIDONE 125 MGCancelled Post Market
00576700SERTAN TAB 125MGPHARMASCIENCE INCTabletPRIMIDONE 125 MGCancelled Post Market
00576719SERTAN TAB 250MGPHARMASCIENCE INCTabletPRIMIDONE 250 MGCancelled Post Market

International API supply for PRIMIDONE

4 valid EDQM Certificates of Suitability from 4 holders. 5 active FDA Drug Master Files.

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