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MEFENAMIC-250 DIN 02230408

Status: Cancelled Post Market
Holder: PRO DOC LIMITEE
Molecule: MEFENAMIC ACID

Health Canada record

Active ingredient(s)MEFENAMIC ACID 250 MG
Dosage formCapsule
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCM01AG01 MEFENAMIC ACID
Original market date06-Aug-1997
Current status date23-Jul-2009
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 MEFENAMIC ACID

DINProductCompanyFormStrengthStatus
02229452MEFENAMICAA PHARMA INCCapsuleMEFENAMIC ACID 250 MGMarketed
02229569MEFENAMIC ACIDAPOTEX INCCapsuleMEFENAMIC ACID 250 MGApproved
02237826DOM-MEFENAMIC ACIDDOMINION PHARMACALCapsuleMEFENAMIC ACID 250 MGCancelled Post Market
02239836NOVO-MEFENAMIC CAPSULES 250MGNOVOPHARM LIMITEDCapsuleMEFENAMIC ACID 250 MGCancelled Pre Market
02231208PMS-MEFENAMIC ACIDPHARMASCIENCE INCCapsuleMEFENAMIC ACID 250 MGCancelled Post Market
00155225PONSTANAA PHARMA INCCapsuleMEFENAMIC ACID 250 MGDormant

Notices of Compliance

NOCDateSubmissionReason
39311997-01-30New Drug Submission (NDS)

International API supply for MEFENAMIC ACID

4 valid EDQM Certificates of Suitability from 4 holders. 8 active FDA Drug Master Files.

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