DORZOLAMIDE-TIMOLOL SOLUTION

Država: Kanada

Jezik: angleščina

Source: Health Canada

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Prenos Lastnosti izdelka (SPC)
30-12-2022

Aktivna sestavina:

DORZOLAMIDE (DORZOLAMIDE HYDROCHLORIDE); TIMOLOL (TIMOLOL MALEATE)

Dostopno od:

JAMP PHARMA CORPORATION

Koda artikla:

S01ED51

INN (mednarodno ime):

TIMOLOL, COMBINATIONS

Odmerek:

20MG; 5MG

Farmacevtska oblika:

SOLUTION

Sestava:

DORZOLAMIDE (DORZOLAMIDE HYDROCHLORIDE) 20MG; TIMOLOL (TIMOLOL MALEATE) 5MG

Pot uporabe:

OPHTHALMIC

Enote v paketu:

15G/50G

Tip zastaranja:

Prescription

Terapevtsko območje:

BETA-ADRENERGIC AGENTS

Povzetek izdelek:

Active ingredient group (AIG) number: 0237301001; AHFS:

Status dovoljenje:

APPROVED

Datum dovoljenje:

2021-11-04

Lastnosti izdelka

                                _Dorzolamide-Timolol_
_ _
_(Dorzolamide Hydrochloride and Timolol Maleate) _
_Page 1 of 35 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
DORZOLAMIDE-TIMOLOL
Dorzolamide Hydrochloride and Timolol Maleate Ophthalmic Solution
Solution, 20 mg / mL Dorzolamide (as Dorzolamide Hydrochloride) and 5
mg / mL Timolol
(as Timolol Maleate), Ophthalmic
Manufacturer’s Standard
Elevated Intraocular Pressure Therapy
Topical Carbonic Anhydrase Inhibitor and Topical Beta-Adrenergic
Blocking Agent
JAMP Pharma Corporation
1310 rue Nobel
Boucherville, Quebec
J4B 5H3, Canada
Date of Initial Authorization:
October 28, 2021
Date of Revision:
December 30, 2022
Submission Control Number: 266282
_Dorzolamide-Timolol_
_ _
_(Dorzolamide Hydrochloride and Timolol Maleate) _
_Page 2 of 35 _
RECENT MAJOR LABEL CHANGES
Not applicable.
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
......
                                
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