Discontinuation report RANITIDINE

Last updated on 2021-04-01 History
Report ID 120746
Drug Identification Number 00740756
Brand name RANITIDINE
Common or Proper name RANITIDINE -300
Company Name PRO DOC LIMITEE
Market Status CANCELLED POST MARKET
Active Ingredient(s) RANITIDINE
Strength(s) 300MG
Dosage form(s) TABLET
Route of administration ORAL ORAL
Packaging size 100
ATC code A02BA
ATC description DRUGS FOR PEPTIC ULCER AND GASTROESOPHAGEAL REFLUX DISEASE (GERD)
Reason for discontinuation Other (Please describe in comments)
Anticipated discontinuation date
Actual discontinuation date
Remaining supply date
Discontinuation status Reversed
Discontinuation decision reversal Yes
Information on remaining supply
Company comments Regulatory issues- Enjeux réglementaires We are looking to re-introduce into the market
Health Canada comments
Tier 3 Status No
Contact Address 2925 BOULEVARD INDUSTRIEL
LAVAL, QUEBEC
CANADA H7L 3W9
Company contact information 2925 BOULEVARD INDUSTRIEL, LAVAL QC, H7L 3W9

Version History

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Version Number Date Updated Language
v6 2021-04-01 French Compare
v5 2021-04-01 English Compare
v4 2020-07-22 French Compare
v3 2020-07-22 English Compare
v2 2020-07-22 French Compare
v1 2020-07-22 English Compare

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