ApprovalTrail

Drug · DIN 00869325

MORPHINE EXTRA-FORTE

No: no longer authorized

The company stopped selling it and its DIN was cancelled. A cancellation is most often a business decision; the record does not say why.

Status Cancelled Post Market since January 6, 2020; first marketed December 31, 1990.
Drug Identification Number (DIN)
00869325
Company (DIN owner)
Pfizer Canada UlcKirkland, Quebec, Canada
Schedule
Narcotics (CDSA I)
Dosage form
Solution
Route
Subcutaneous; Intramuscular; Intravenous
Therapeutic class (ATC)
Morphine N02AA01
Class
Human
Record last updated
March 22, 2025

Active ingredients

As listed in the Drug Product Database.

IngredientStrengthPer
MORPHINE SULFATE50 MGML