Product information

From Health Canada

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:

2002-05-16

Original market date: See footnote 1

1979-12-31

Product name:

POLLINEX R

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DIN:

00464988

Product Monograph/Veterinary Labelling:

Date: 2017-09-29 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company:

ALLERGY THERAPEUTICS (UK) LTD
Dominion Way
Worthing
West Sussex
United Kingdom BN14 8SA

Class:

Human

Dosage form(s):

Liquid

Route(s) of administration:

Subcutaneous

Number of active ingredient(s):

4

Schedule(s):

Schedule D

 

American Hospital Formulary Service (AHFS): See footnote 3

92:05.00* See footnote6 

Anatomical Therapeutic Chemical (ATC): See footnote 4

V01AA02 GRASS POLLEN

Active ingredient group (AIG) number:See footnote5

0447001001

List of active ingredient(s)
Active ingredient(s) See footnote8 Strength
MODIFIED RAGWEED TYROSINE ADSORBATE 1400 UNIT / ML
MODIFIED RAGWEED TYROSINE ADSORBATE 210 UNIT / ML
MODIFIED RAGWEED TYROSINE ADSORBATE 4300 UNIT / ML
MODIFIED RAGWEED TYROSINE ADSORBATE 500 UNIT / ML
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