Discontinuation report ACT FINASTERIDE

Last updated on 2018-10-22 History
Report ID 65281
Drug Identification Number 02354462
Brand name ACT FINASTERIDE
Common or Proper name FINASTERIDE
Company Name ACTAVIS PHARMA COMPANY
Market Status CANCELLED POST MARKET
Active Ingredient(s) FINASTERIDE
Strength(s) 5MG
Dosage form(s) TABLET
Route of administration ORAL
Packaging size 30
ATC code G04CB
ATC description DRUGS USED IN BENIGN PROSTATIC HYPERTROPHY
Reason for discontinuation Business reasons
Anticipated discontinuation date
Actual discontinuation date 2018-05-31
Remaining supply date 2018-05-31
Discontinuation status Discontinued
Discontinuation decision reversal No
Information on remaining supply
Company comments Transitioned. TEVA available
Health Canada comments
Tier 3 Status No
Contact Address 30 NOVOPHARM COURT
TORONTO, ONTARIO
CANADA M1B 2K9
Company contact information

Version History

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Version Number Date Updated Language
v1 2018-10-22 English Compare
v2 2018-10-22 French Compare

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