SANDOZ TIMOLOL SOLUTION

Maa: Kanada

Kieli: englanti

Lähde: Health Canada

Aktiivinen ainesosa:

TIMOLOL (TIMOLOL MALEATE)

Saatavilla:

SANDOZ CANADA INCORPORATED

ATC-koodi:

S01ED01

INN (Kansainvälinen yleisnimi):

TIMOLOL

Annos:

0.5%

Lääkemuoto:

SOLUTION

Koostumus:

TIMOLOL (TIMOLOL MALEATE) 0.5%

Antoreitti:

OPHTHALMIC

Kpl paketissa:

5ML/10ML

Prescription tyyppi:

Prescription

Terapeuttinen alue:

BETA-ADRENERGIC AGENTS

Tuoteyhteenveto:

Active ingredient group (AIG) number: 0131275002; AHFS:

Valtuutuksen tilan:

APPROVED

Valtuutus päivämäärä:

1999-10-07

Valmisteyhteenveto

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_Sandoz Timolol _
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PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
Pr
SANDOZ TIMOLOL
Timolol Maleate Ophthalmic Solution
Solution, 0.25%, 0.5% w/v timolol (as timolol maleate), ophthalmic
USP
Antiglaucoma Preparations and Miotics
Sandoz Canada Inc.
110 rue de Lauzon,
Boucherville, QC,
J4B 1E6
Date of Initial Authorization:
AUG 22, 2005
Date of Revision:
MAR 07, 2024
Submission Control Number:
283616
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_Sandoz timolol _
_Page 2 of 25_
RECENT MAJOR LABEL CHANGES
6
Dosage Forms, Strengths, Composition and Packaging
03/2024
TABLE OF CONTENTS
SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF
AUTHORIZATION ARE NOT LISTED
.
RECENT MAJOR LABEL CHANGES
..........................................................................................
2
TABLE OF CONTENTS
............................................................................................................
2
PART I: HEALTH PROFESSIONAL INFORMATION
.................................................................... 4
1
INDICATIONS
.............................................................................................................
4
1.1 Pediatrics
......................................................................................................................
4
1.2 Geriatrics
......................................................................................................................
4
2
CONTRAINDICATIONS
................................................................................................
4
4
DOSAGE AND ADMINISTRATION
................................................................................
4
4.1 Dosing Considerations
.................................................................................................
4
4.2 Recommended Dose and Dosage Adjustment
............................................................ 5
4.4 Administration
.............................................................................................................
5
4.5 Missed Dose