SANDOZ TIMOLOL SOLUTION

Negara: Kanada

Bahasa: Inggris

Sumber: Health Canada

Beli Sekarang

Unduh Karakteristik produk (SPC)
07-03-2024

Bahan aktif:

TIMOLOL (TIMOLOL MALEATE)

Tersedia dari:

SANDOZ CANADA INCORPORATED

Kode ATC:

S01ED01

INN (Nama Internasional):

TIMOLOL

Dosis:

0.5%

Bentuk farmasi:

SOLUTION

Komposisi:

TIMOLOL (TIMOLOL MALEATE) 0.5%

Rute administrasi :

OPHTHALMIC

Unit dalam paket:

5ML/10ML

Jenis Resep:

Prescription

Area terapi:

BETA-ADRENERGIC AGENTS

Ringkasan produk:

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

Status otorisasi:

APPROVED

Tanggal Otorisasi:

1999-10-07

Karakteristik produk

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_Sandoz Timolol _
_Page 1 of 25_
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

                                
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