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ENABLEX DIN 02273225

Status: Marketed
Holder: SEARCHLIGHT PHARMA INC
Molecule: DARIFENACIN (DARIFENACIN HYDROBROMIDE)
Available to quote

Health Canada record

Active ingredient(s)DARIFENACIN (DARIFENACIN HYDROBROMIDE) 15 MG
Dosage formTablet (Extended-Release)
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCG04BD10 DARIFENACIN
Original market date06-Apr-2006
Current status date02-Apr-2019
SourceHealth Canada DPD

Establishment licence of the holder

Searchlight Pharma Inc — licence 102247, currently licensed, last inspection rating C (2024-10-10).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing DARIFENACIN (DARIFENACIN HYDROBROMIDE)

DINProductCompanyFormStrengthStatus
02452510APO-DARIFENACINAPOTEX INCTablet (Extended-Release)DARIFENACIN (DARIFENACIN HYDROBROMIDE) 7.5 MGMarketed
02452529APO-DARIFENACINAPOTEX INCTablet (Extended-Release)DARIFENACIN (DARIFENACIN HYDROBROMIDE) 15 MGMarketed
02273217ENABLEXSEARCHLIGHT PHARMA INCTablet (Extended-Release)DARIFENACIN (DARIFENACIN HYDROBROMIDE) 7.5 MGMarketed
02491869JAMP DARIFENACINJAMP PHARMA CORPORATIONTablet (Extended-Release)DARIFENACIN (DARIFENACIN HYDROBROMIDE) 7.5 MGMarketed
02491877JAMP DARIFENACINJAMP PHARMA CORPORATIONTablet (Extended-Release)DARIFENACIN (DARIFENACIN HYDROBROMIDE) 15 MGMarketed

Notices of Compliance

NOCDateSubmissionReason
218422019-02-11New Drug Submission (NDS)A CHANGE IN PRODUCT OWNERSHIP FROM MJERUS LABS TO SEARCHLIGHT PHARMA INC., AND TO ADD A PVC-PVDC WITH ALUMINUM FOIL BLISTER PACK OF 7 TABLETS FOR THE 7.5 MG TABLET
142902013-04-16New Drug Submission (NDS)Manufacturer name change
76102005-11-14New Drug Submission (NDS)
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