Product information

Current status:

Cancelled Post Market

Current status date:

2005-08-01

Original market date: ^{See footnote 1}

1966-12-31

Product name:

OMNI-TUSS SUS

DIN:

00815136 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):

Suspension

Route(s) of administration:

Oral

Number of active ingredient(s):

5

Schedule(s):

Narcotic (CDSA I)

American Hospital Formulary Service (AHFS): ^{See footnote 3}

48:08.00 

Anatomical Therapeutic Chemical (ATC): ^{See footnote 4}

R05FA02 OPIUM DERIVATIVES AND EXPECTORANTS

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

0521133001