Product information

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Current status:

Marketed

Current status date:

2016-02-03

Original market date: See footnote 1

2002-04-09

Product name:

MANNITOL INJECTION

DIN:

02243176 Electronic product monograph is not available

Company: 

FRESENIUS KABI CANADA LTD
165 Galaxy Blvd, Suite 100
Toronto
Ontario
Canada  M9W 0C8

Class: 

Human

Dosage form(s):

Solution

Route(s) of administration:

Intravenous

Number of active ingredient(s):

1

Schedule(s):

Ethical  

Biosimilar Biologic Drug:

No

American Hospital Formulary Service (AHFS): See footnote 3

40:28.12   OSMOTIC DIURETICS

Anatomical Therapeutic Chemical (ATC): See footnote 4

B05BC01  MANNITOL

Active ingredient group (AIG) number:See footnote 5

0103277001

List of active ingredient(s)
Active ingredient(s) Strength
MANNITOL 25 %

Application information

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