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ONSOLIS - Health Canada Drug Approval Details
Approvals
/
Health Canada
/
ONSOLIS
Authorized
STANDARD
ONSOLIS
Meda AB
🇨🇦 Health Canada
Approval Date
Jul 4, 2025
Approval ID
d59e18471af054b3
Company
Meda AB
Type
Standard
Approval Details
Approval Id
d59e18471af054b3
Drug Approval Canada Name
ONSOLIS
Product Name
ONSOLIS
Status
Cancelled Post Market
Status Date
2013-01-31
Original Market Date
2011-08-22
Din
02350718
Drug Class
Human
Dosage Form
Film, Soluble
Route Of Administration
Buccal
Schedule
Narcotic (CDSA I)
Ahfs
28:08.08
Atc Original
N02AB03 FENTANYL
Atc Name
n 02 ab 03
Aig Number
0123302020
Company Name
Meda AB
Company Address
Pipers Väg 2a, Solna, --, Sweden, 17009
Company Detail Path
/organization/meda-ab
Company Information
Pharmaceutical Company Name
Meda AB
Country Name
Sweden
Website
http://meda.se
Active Ingredients
FENTANYL (FENTANYL CITRATE)
800 MCG
Authorized
Quick Info
Agency
Health Canada
Country
🇨🇦
Approval Date
Jul 4, 2025
Approval ID
d59e18471af054b3
Type
Standard
Back to Health Canada Approvals