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NALOXONE HYDROCHLORIDE INJECTION DIN 02572214

Status: Approved
Holder: JUNO PHARMA CANADA INC.
Molecule: NALOXONE HYDROCHLORIDE (NALOXONE HYDROCHLORIDE DIHYDRATE)

Health Canada record

Active ingredient(s)NALOXONE HYDROCHLORIDE (NALOXONE HYDROCHLORIDE DIHYDRATE) 0.4 MG
Dosage formSolution
RouteSubcutaneous; Intravenous; Intramuscular
ScheduleETHICAL
ClassHuman
ATCV03AB15 NALOXONE
Original market date
Current status date09-Oct-2026
SourceHealth Canada DPD

Establishment licence of the holder

Juno Pharma Canada Inc. — licence 3-002916, currently licensed, last inspection rating C (2025-11-24).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing NALOXONE HYDROCHLORIDE (NALOXONE HYDROCHLORIDE DIHYDRATE)

DINProductCompanyFormStrengthStatus
02455935INJECTABLE NALOXONE HYDROCHLORIDEOMEGA LABORATORIES LIMITEDSolutionNALOXONE HYDROCHLORIDE (NALOXONE HYDROCHLORIDE DIHYDRATE) 0.4 MGMarketed
02464357INJECTABLE NALOXONE HYDROCHLORIDEOMEGA LABORATORIES LIMITEDSolutionNALOXONE HYDROCHLORIDE (NALOXONE HYDROCHLORIDE DIHYDRATE) 1 MGApproved
02393034NALOXONE HYDROCHLORIDE INJECTIONOMEGA LABORATORIES LIMITEDSolutionNALOXONE HYDROCHLORIDE (NALOXONE HYDROCHLORIDE DIHYDRATE) 0.4 MGMarketed
02393042NALOXONE HYDROCHLORIDE INJECTIONOMEGA LABORATORIES LIMITEDSolutionNALOXONE HYDROCHLORIDE (NALOXONE HYDROCHLORIDE DIHYDRATE) 1 MGMarketed
02382482NALOXONE HYDROCHLORIDE INJECTION USPHIKMA CANADA LIMITEDSolutionNALOXONE HYDROCHLORIDE (NALOXONE HYDROCHLORIDE DIHYDRATE) 0.4 MGMarketed
02459892NALOXONE HYDROCHLORIDE INJECTION, USPSTRIDES PHARMA CANADA INCSolutionNALOXONE HYDROCHLORIDE (NALOXONE HYDROCHLORIDE DIHYDRATE) 0.4 MGApproved
02382601NALOXONE HYDROCHLORIDE INJECTION SDZ PRESERVATIVE FREESANDOZ CANADA INCORPORATEDSolutionNALOXONE HYDROCHLORIDE (NALOXONE HYDROCHLORIDE DIHYDRATE) 0.4 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
384392026-10-09Abbreviated New Drug Submission (ANDS)
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