Product information

Current status:

Cancelled Post Market

Current status date:

2009-07-23

Original market date: ^{See footnote 1}

1996-12-31

Product name:

KETOPROFEN-E ECT 100MG

DIN:

02084198 Electronic product monograph is not available

Company:

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

Class:

Human

Dosage form(s):

Tablet (Enteric-Coated)

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}

M01AE03 KETOPROFEN

Active ingredient group (AIG) number:^{See footnote5}

0110497002