Drug Report History

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Below you will find the report version history. When a report is updated, a new version of the report is created. The report history allows you to see the changes between versions. You can select two versions of the report to compare. The fields that were changed between versions will be highlighted in yellow.

The translation of reports creates two separate versions which is why some reports may not seem to have any differences. In this case, only the language field below will be highlighted in yellow.

Version v4-FR Version v1-EN
Language French English
Date Updated 2018-12-28 2018-09-08
Drug Identification Number 02460912 02460912
Brand name APO-PHENYTOIN SODIUM APO-PHENYTOIN SODIUM
Common or Proper name PHENYTOIN PHENYTOIN
Company Name AA PHARMA INC AA PHARMA INC
Ingredients PHENYTOIN SODIUM PHENYTOIN SODIUM
Strength(s) 100MG 100MG
Dosage form(s) CAPSULE CAPSULE
Route of administration ORAL ORAL
Packaging size 100 BTL 100 BTL
ATC code N03AB N03AB
ATC description ANTIEPILEPTICS ANTIEPILEPTICS
Reason for discontinuation Business reasons Business reasons
Anticipated discontinuation date 2019-04-03
Actual discontinuation date 2018-10-29
Remaining supply date 2018-10-29 2019-04-03
Discontinuation status Discontinued To be discontinued
Discontinuation decision reversal no no
Tier 3 Status No No
Information on remaining supply
Company comments
Health Canada comments