Discontinuation report RANITIDINE

Last updated on 2019-03-12 History
Report ID 69784
Drug Identification Number 02385961
Brand name RANITIDINE
Common or Proper name RANITIDINE
Company Name SIVEM PHARMACEUTICALS ULC
Market Status CANCELLED POST MARKET
Active Ingredient(s) RANITIDINE
Strength(s) 300MG
Dosage form(s) TABLET
Route of administration ORAL
Packaging size 30
ATC code A02BA
ATC description DRUGS FOR PEPTIC ULCER AND GASTROESOPHAGEAL REFLUX DISEASE (GERD)
Reason for discontinuation Business reasons
Anticipated discontinuation date 2019-02-25
Actual discontinuation date 2019-02-27
Remaining supply date 2019-04-01
Discontinuation status Discontinued
Discontinuation decision reversal No
Information on remaining supply
Company comments Pack size discontinuation only
Health Canada comments
Tier 3 Status No
Contact Address 4705 DOBRIN STREET
SAINT-LAURENT, QUEBEC
CANADA H4R 2P7
Company contact information

Version History

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Version Number Date Updated Language
v1 2018-12-17 English Compare
v2 2018-12-17 French Compare
v3 2019-01-07 English Compare
v4 2019-01-07 French Compare
v5 2019-01-14 English Compare
v6 2019-01-14 French Compare
v7 2019-01-28 English Compare
v8 2019-01-28 French Compare
v9 2019-02-18 English Compare
v10 2019-02-18 French Compare
v11 2019-02-22 English Compare
v12 2019-02-22 French Compare
v13 2019-03-12 English Compare
v14 2019-03-12 French Compare

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