Product information

Current status:

Cancelled Post Market

Current status date:

2000-07-28

Original market date: ^{See footnote 1}

1997-10-21

Product name:

RHODIAPROX - 500MG/SUP

DIN:

02229690 Electronic product monograph is not available

Company:

RHODIAPHARM INC
2150 Boul. St. Elzear Ouest
Laval
Quebec
Canada H7L 4A8

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}

M01AE02 NAPROXEN

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

0109634003