Drug Report History

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Version v3-EN Version v1-EN
Language English English
Date Updated 2020-11-03 2020-11-02
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 1 VIAL 50ML 1 VIAL 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 discontinuation Manufacturing issues Manufacturing issues
Anticipated discontinuation date
Actual discontinuation date 2020-11-02 2020-11-02
Remaining supply date 2020-11-02 2020-11-02
Discontinuation status Discontinued To be discontinued
Discontinuation decision reversal no no
Tier 3 Status No No
Information on remaining supply
Company comments PrFamotidine Omega 10mg/mL as a substitute for PrRanitidine Injection USP 25 mg/mL PrFamotidine Omega 10mg/mL as a substitute for PrRanitidine Injection USP 25 mg/mL
Health Canada comments