Product information

Current status:

Cancelled Post Market

Current status date:

2002-07-31

Original market date: ^{See footnote 1}

1973-12-31

Product name:

SODIUM FLUORIDE DPS 6.9MG

DIN:

00179191 Electronic product monograph is not available

Company:

STANLEY PHARMACEUTICALS, A DIVISION OF VITA HEALTH PRODUCTS INC.
150 Beghin Avenue
Winnipeg
Manitoba
Canada R2J 3W2

Class:

Human

Dosage form(s):

Liquid

Route(s) of administration:

Oral

Number of active ingredient(s):

1

Schedule(s):

OTC

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

34:00.00 

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

A01AA01 SODIUM FLUORIDE

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

0107147002