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JAMP MYCOPHENOLIC ACID DIN 02518538

Status: Marketed
Holder: JAMP PHARMA CORPORATION
Molecule: MYCOPHENOLIC ACID (MYCOPHENOLATE SODIUM)

Health Canada record

Active ingredient(s)MYCOPHENOLIC ACID (MYCOPHENOLATE SODIUM) 180 MG
Dosage formTablet (Enteric-Coated)
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCL04AA06 MYCOPHENOLIC ACID
Original market date10-Nov-2021
Current status date13-Mar-2025
SourceHealth Canada DPD

Establishment licence of the holder

Jamp Pharma Corporation — licence 100590, currently licensed, last inspection rating C (2025-01-13).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing MYCOPHENOLIC ACID (MYCOPHENOLATE SODIUM)

DINProductCompanyFormStrengthStatus
02372738APO-MYCOPHENOLIC ACIDAPOTEX INCTablet (Enteric-Coated)MYCOPHENOLIC ACID (MYCOPHENOLATE SODIUM) 180 MGMarketed
02372746APO-MYCOPHENOLIC ACIDAPOTEX INCTablet (Enteric-Coated)MYCOPHENOLIC ACID (MYCOPHENOLATE SODIUM) 360 MGMarketed
02518511JAMP MYCOPHENOLIC ACIDJAMP PHARMA CORPORATIONTablet (Enteric-Coated)MYCOPHENOLIC ACID (MYCOPHENOLATE SODIUM) 360 MGMarketed
02511681MAR-MYCOPHENOLIC ACIDMARCAN PHARMACEUTICALS INCTablet (Enteric-Coated)MYCOPHENOLIC ACID (MYCOPHENOLATE SODIUM) 360 MGMarketed
02511673MAR-MYCOPHENOLIC ACIDMARCAN PHARMACEUTICALS INCTablet (Enteric-Coated)MYCOPHENOLIC ACID (MYCOPHENOLATE SODIUM) 180 MGMarketed
02264560MYFORTICNOVARTIS PHARMACEUTICALS CANADA INCTablet (Delayed-Release)MYCOPHENOLIC ACID (MYCOPHENOLATE SODIUM) 180 MGMarketed
02264579MYFORTICNOVARTIS PHARMACEUTICALS CANADA INCTablet (Delayed-Release)MYCOPHENOLIC ACID (MYCOPHENOLATE SODIUM) 360 MGMarketed
02465817SANDOZ MYCOPHENOLIC ACIDSANDOZ CANADA INCORPORATEDTablet (Enteric-Coated)MYCOPHENOLIC ACID (MYCOPHENOLATE SODIUM) 360 MGCancelled Pre Market
02465809SANDOZ MYCOPHENOLIC ACIDSANDOZ CANADA INCORPORATEDTablet (Enteric-Coated)MYCOPHENOLIC ACID (MYCOPHENOLATE SODIUM) 180 MGCancelled Pre Market

Notices of Compliance

NOCDateSubmissionReason
328792024-03-14Abbreviated New Drug Submission (ANDS)
263972021-08-06Abbreviated New Drug Submission (ANDS)LICENSING AGREEMMENT BETWEEN TWO COMPANIES
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