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MOMETASONE DIN 02551756

Status: Marketed
Holder: SIVEM PHARMACEUTICALS ULC
Molecule: MOMETASONE FUROATE (MOMETASONE FUROATE MONOHYDRATE)

Health Canada record

Active ingredient(s)MOMETASONE FUROATE (MOMETASONE FUROATE MONOHYDRATE) 50 MCG
Dosage formSpray (Metered-Dose)
RouteNasal
SchedulePRESCRIPTION
ClassHuman
ATCR01AD09 MOMETASONE
Original market date06-Jun-2025
Current status date06-Jun-2025
SourceHealth Canada DPD

Establishment licence of the holder

Sivem Pharmaceuticals ULC — licence 101965, currently licensed, last inspection rating C (2025-02-04).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing MOMETASONE FUROATE (MOMETASONE FUROATE MONOHYDRATE)

DINProductCompanyFormStrengthStatus
02519127MOMETASONESANIS HEALTH INCSpray (Metered-Dose)MOMETASONE FUROATE (MOMETASONE FUROATE MONOHYDRATE) 50 MCGMarketed
02449811SANDOZ MOMETASONESANDOZ CANADA INCORPORATEDSpray (Metered-Dose)MOMETASONE FUROATE (MOMETASONE FUROATE MONOHYDRATE) 50 MCGMarketed
02455870MOSASPRAYSANDOZ CANADA INCORPORATEDSpray (Metered-Dose)MOMETASONE FUROATE (MOMETASONE FUROATE MONOHYDRATE) 50 MCGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
340512024-09-20Abbreviated New Drug Submission (ANDS)Administrative: Licensing Agreement between two manufacturers
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