Product information

From Health Canada

Current status:

Cancelled Post Market

Current status date:

2014-07-24

Original market date: See footnote 1

1986-12-31

Product name:

IBUPROFEN-600 TAB 600MG

DIN:

00658804 Electronic product monograph is not available

Company:

PRO DOC LIMITEE
2925 Boulevard Industriel
Laval
Quebec
Canada H7L 3W9

Class:

Human

Dosage form(s):

Tablet

Route(s) of administration:

Oral

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

M01AE01 IBUPROFEN

Active ingredient group (AIG) number:See footnote5

0108883003

List of active ingredient(s)
Active ingredient(s) Strength
IBUPROFEN 600 MG
Version 4.0.2
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