Product information

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Current status:

Marketed

Current status date:

2005-08-06

Original market date: See footnote 1

1993-12-31

Product name:

SANDOZ PREDNISOLONE

DIN:

01916203 Electronic product monograph is not available

Company: 

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

Class: 

Human

Dosage form(s):

Suspension

Route(s) of administration:

Ophthalmic

Number of active ingredient(s):

1

Schedule(s):

Prescription  

Biosimilar Biologic Drug:

No

American Hospital Formulary Service (AHFS): See footnote 3

52:08.08   CORTICOSTEROIDS

Anatomical Therapeutic Chemical (ATC): See footnote 4

S01BA04  PREDNISOLONE

Active ingredient group (AIG) number:See footnote 5

0106295001

List of active ingredient(s)
Active ingredient(s) Strength
PREDNISOLONE ACETATE 1 %

Application information

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