Product information

Current status:

Cancelled Post Market

Current status date:

2012-01-23

Original market date: ^{See footnote 1}

1992-12-31

Product name:

HYDROMORPHONE HYDROCHLORIDE SUP 3MG

DIN:

01979914 Electronic product monograph is not available

Company:

SANDOZ CANADA INCORPORATED
110 Rue De Lauzon
Boucherville
Quebec
Canada J4B 1E6

Class:

Human

Dosage form(s):

Suppository

Route(s) of administration:

Rectal

Number of active ingredient(s):

1

Schedule(s):

Narcotic (CDSA I)

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

28:08.08 

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

N02AA03 HYDROMORPHONE

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

0108698002