Product information

From Health Canada

New search

The product monograph is developed by a drug sponsor according to guidelines published by Health Canada that provide direction on the content and format. The veterinary labelling is developed by the drug sponsor according to the Food and Drug Regulations. While Health Canada reviews the product monograph or the veterinary labelling as part of the drug review process, it remains the responsibility of the drug sponsor to ensure that the product monograph or the veterinary labelling is complete and accurate.

Current status:

Marketed

Current status date:

2019-06-05

Original market date: See footnote 1

2019-06-05

Product name:

STRAMUCIN

Help on accessing alternative formats, such as Portable Document Format (PDF), Microsoft Word and PowerPoint (PPT) files, can be obtained in the alternate format help section .

DIN:

02483459

Product Monograph/Veterinary Labelling:

Date: 2018-11-21 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company: 

GLENMARK PHARMACEUTICALS CANADA INC.
1600 Steeles Ave. W., Suite 407
Concord
Ontario
Canada  L4K 4M2

Class: 

Human

Dosage form(s):

Cream

Route(s) of administration:

Topical

Number of active ingredient(s):

1

Schedule(s):

OTC  

Biosimilar Biologic Drug:

No

American Hospital Formulary Service (AHFS): See footnote 3

84:04.04   ANTIBIOTICS

Anatomical Therapeutic Chemical (ATC): See footnote 4

D06AX09  MUPIROCIN

Active ingredient group (AIG) number:See footnote 5

0117081001

List of active ingredient(s)
Active ingredient(s) Strength
MUPIROCIN (MUPIROCIN CALCIUM) 2 % / W/W

Application information

Related information

Contact us

Version 3.8.0
Date modified: