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THIOTEPA - (PWS 15 MG/VIAL) DIN 02174391

Status: Cancelled Post Market
Holder: WYETH CANADA
Molecule: THIOTEPA

Health Canada record

Active ingredient(s)THIOTEPA 15 MG
Dosage formPowder For Solution
RouteIntracavitary; Intravesicular; Intravenous
SchedulePRESCRIPTION
ClassHuman
ATCL01AC01 THIOTEPA
Original market date25-Aug-1997
Current status date15-Sep-2004
SourceHealth Canada DPD

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing THIOTEPA

DINProductCompanyFormStrengthStatus
02567059TEPADINAADIENNE SAPowder For SolutionTHIOTEPA 200 MGApproved
02462680TEPADINAADIENNE SAPowder For SolutionTHIOTEPA 15 MGMarketed
02462702TEPADINAADIENNE SAPowder For SolutionTHIOTEPA 100 MGMarketed
02526417THIOTEPA FOR INJECTION USPSTERIMAX INCPowder For SolutionTHIOTEPA 15 MGMarketed
02526425THIOTEPA FOR INJECTION USPSTERIMAX INCPowder For SolutionTHIOTEPA 100 MGMarketed
02536862THIOTEPA FOR INJECTION, BPHIKMA CANADA LIMITEDPowder For SolutionTHIOTEPA 15 MGMarketed
02536870THIOTEPA FOR INJECTION, BPHIKMA CANADA LIMITEDPowder For SolutionTHIOTEPA 100 MGMarketed
02523906TEPADINAADIENNE SAPowder For SolutionTHIOTEPA 400 MGDormant
00237035THIO TEPA INJ 15MG/VIALLEDERLE CYANAMID CANADA INC.Powder For SolutionTHIOTEPA 15 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
36172003-04-23New Drug Submission (NDS)MANUFACTURER NAME CHANGE

International API supply for THIOTEPA

7 active FDA Drug Master Files.

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