Drug Report History

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Version v9-FR Version v4-EN
Language French English
Date Updated 2023-11-17 2020-09-15
Drug Identification Number 02256711 02256711
Brand name RANITIDINE INJECTION USP RANITIDINE INJECTION USP
Common or Proper name RANITIDINE RANITIDINE
Company Name SANDOZ CANADA INCORPORATED SANDOZ CANADA INCORPORATED
Ingredients RANITIDINE RANITIDINE
Strength(s) 50MG 50MG
Dosage form(s) SOLUTION SOLUTION
Route of administration INTRAMUSCULAR INTRAVENOUS INTRAMUSCULAR INTRAVENOUS INTRAMUSCULAR INTRAVENOUS INTRAMUSCULAR INTRAVENOUS
Packaging size 50ML 50ML
ATC code A02BA A02BA
ATC description DRUGS FOR PEPTIC ULCER AND GASTROESOPHAGEAL REFLUX DISEASE (GERD) DRUGS FOR PEPTIC ULCER AND GASTROESOPHAGEAL REFLUX DISEASE (GERD)
Reason for shortage Requirements related to complying with good manufacturing practices. Requirements related to complying with good manufacturing practices.
Anticipated start date 2020-09-14 2020-09-14
Actual start date
Estimated end date Unknown 2020-09-28
Actual end date 2021-03-01
Shortage status Resolved Actual shortage
Tier 3 Status No No
Company comments
Health Canada comments