Product information

From Health Canada

Current status:

Cancelled Post Market

Current status date:

2003-07-22

Original market date: See footnote 1

1979-12-31

Product name:

ORUDIS 100

DIN:

01926411 Electronic product monograph is not available

Company:

AVENTIS PHARMA INC
2905 Place Louis-R. Renaud
Laval
Quebec
Canada H7V 0A3

Class:

Human

Dosage form(s):

Suppository

Route(s) of administration:

Rectal

Number of active ingredient(s):

1

Schedule(s):

Prescription

 

American Hospital Formulary Service (AHFS): See footnote 3

28:08.04.92 

Anatomical Therapeutic Chemical (ATC): See footnote 4

M01AE03 KETOPROFEN

Active ingredient group (AIG) number:See footnote5

0110497002

List of active ingredient(s)
Active ingredient(s) See footnote8 Strength
KETOPROFEN 100 MG
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