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HYDROMORPHONE HYDROCHLORIDE INJECTION HP FORTE - Health Canada Drug Approval Details
Approvals
/
Health Canada
/
HYDROMORPHONE HYDROCHLORIDE INJECTION HP FORTE
Authorized
STANDARD
HYDROMORPHONE HYDROCHLORIDE INJECTION HP FORTE
Sterimax Inc
🇨🇦 Health Canada
Approval Date
Jul 4, 2025
Approval ID
57ec3d0175f1ca80
Company
Sterimax Inc
Type
Standard
Approval Details
Approval Id
57ec3d0175f1ca80
Drug Approval Canada Name
HYDROMORPHONE HYDROCHLORIDE INJECTION HP FORTE
Product Name
HYDROMORPHONE HYDROCHLORIDE INJECTION HP FORTE
Status
Marketed
Status Date
2018-06-20
Original Market Date
2018-06-20
Din
02468468
Drug Class
Human
Dosage Form
Solution
Route Of Administration
Intravenous , Intramuscular , Subcutaneous
Schedule
Narcotic (CDSA I)
Ahfs
28:08.08
Atc Original
N02AA03 HYDROMORPHONE
Atc Name
n 02 aa 03
Aig Number
0108698016
Company Name
Sterimax Inc
Company Address
2770 Portland Drive, Oakville, Ontario, Canada, L6H 6R4
Active Ingredients
HYDROMORPHONE HYDROCHLORIDE
100 MG / ML
Authorized
Quick Info
Agency
Health Canada
Country
🇨🇦
Approval Date
Jul 4, 2025
Approval ID
57ec3d0175f1ca80
Type
Standard
Back to Health Canada Approvals
