Discontinuation report HYDROMORPHONE HYDROCHLORIDE INJECTION USP

Last updated on 2019-09-09 History
Report ID 77142
Drug Identification Number 02382636
Brand name HYDROMORPHONE HYDROCHLORIDE INJECTION USP
Common or Proper name Hydromorphone
Company Name PFIZER CANADA ULC
Market Status MARKETED
Active Ingredient(s) HYDROMORPHONE HYDROCHLORIDE
Strength(s) 10MG
Dosage form(s) SOLUTION
Route of administration INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Packaging size 10x1mL vial
ATC code N02AA
ATC description OPIOIDS
Reason for discontinuation Business reasons
Anticipated discontinuation date
Actual discontinuation date 2019-09-01
Remaining supply date 2019-09-01
Discontinuation status Discontinued
Discontinuation decision reversal No
Information on remaining supply
Company comments
Health Canada comments
Tier 3 Status No
Contact Address 17300 TRANS-CANADA HIGHWAY
KIRKLAND, QUEBEC
CANADA H9J 2M5
Company contact information Customer Service / service à la clientèle : 1-888-999-8750 Email / courriel: PharmaCustomerServiceDept@pfizer.com

Version History

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Version Number Date Updated Language
v4 2019-09-09 French Compare
v3 2019-09-09 English Compare
v2 2019-02-28 French Compare
v1 2019-02-28 English Compare

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