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HYDROMORPHONE HYDROCHLORIDE INJECTION, USP - Health Canada Drug Approval Details
Approvals
/
Health Canada
/
HYDROMORPHONE HYDROCHLORIDE INJECTION, USP
Authorized
STANDARD
HYDROMORPHONE HYDROCHLORIDE INJECTION, USP
fresenius kabi canada ltd
🇨🇦 Health Canada
Approval Date
Jul 4, 2025
Approval ID
b5d6d2e1fe70694d
Company
fresenius kabi canada ltd
Type
Standard
Approval Details
Approval Id
b5d6d2e1fe70694d
Drug Approval Canada Name
HYDROMORPHONE HYDROCHLORIDE INJECTION, USP
Product Name
HYDROMORPHONE HYDROCHLORIDE INJECTION, USP
Status
Marketed
Status Date
2020-11-10
Original Market Date
2020-11-10
Din
02491699
Drug Class
Human
Dosage Form
Solution
Route Of Administration
Subcutaneous , Intramuscular , Intravenous
Schedule
Narcotic (CDSA I)
Ahfs
28:08.08
Atc Original
N02AA03 HYDROMORPHONE
Atc Name
n 02 aa 03
Aig Number
0108698003
Company Name
fresenius kabi canada ltd
Company Address
165 Galaxy Blvd, Suite 100, Toronto, Ontario, Canada, M9W 0C8
Active Ingredients
HYDROMORPHONE HYDROCHLORIDE
2 MG / ML
Authorized
Quick Info
Agency
Health Canada
Country
🇨🇦
Approval Date
Jul 4, 2025
Approval ID
b5d6d2e1fe70694d
Type
Standard
Back to Health Canada Approvals