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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:

2014-06-30

Original market date: See footnote 1

1993-12-31

Product name:

SURVANTA

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:

02016109

Product Monograph/Veterinary Labelling:

Date: 2018-01-05 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company: 

ABBVIE CORPORATION
8401 Trans-Canada Highway
Saint-Laurent
Quebec
Canada  H4S 1Z1

Class: 

Human

Dosage form(s):

Suspension

Route(s) of administration:

Intratracheal

Number of active ingredient(s):

1

Schedule(s):

Prescription  

Biosimilar Biologic Drug:

No

American Hospital Formulary Service (AHFS): See footnote 3

48:36.00   PULMONARY SURFACTANTS

Anatomical Therapeutic Chemical (ATC): See footnote 4

R07AA02  NATURAL PHOSPHOLIPIDS

Active ingredient group (AIG) number:See footnote 5

0124200001

List of active ingredient(s)
Active ingredient(s) Strength
BERACTANT 25 MG / ML

Application information

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