Discontinuation report NALOXONE HYDROCHLORIDE INJECTION

Last updated on 2017-08-19 History
Report ID 19858
Drug Identification Number 02393034
Brand name NALOXONE HYDROCHLORIDE INJECTION
Common or Proper name Naloxone Hydrochloride Injection
Company Name OMEGA LABORATORIES LIMITED
Market Status DORMANT
Active Ingredient(s) NALOXONE HYDROCHLORIDE
Strength(s) 0.4MG
Dosage form(s) SOLUTION
Route of administration INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Packaging size 1mL vial
ATC code V03AB
ATC description ALL OTHER THERAPEUTIC PRODUCTS
Reason for discontinuation Other (Please describe in comments)
Anticipated discontinuation date 2017-08-18
Actual discontinuation date 2017-08-18
Remaining supply date 2017-08-18
Discontinuation status Discontinued
Discontinuation decision reversal No
Information on remaining supply Replaced by DIN number 02455935 (Ethical)
Company comments Replaced by DIN number 02455935 (Ethical)
Health Canada comments
Contact Address 11177 HAMON
MONTREAL, QUEBEC
CANADA H3M 3E4
Company contact information info@omegalaboratory.com - 1-800-363-0584

Version History

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Version Number Date Updated Language
v5 2017-08-19 English Compare
v4 2017-08-18 French Compare
v3 2017-08-18 English Compare
v2 2017-08-18 English Compare
v1 2017-08-18 English Compare