VOLTAREN OPHTHA SOLUTION

देश: कनाडा

भाषा: अंग्रेज़ी

स्रोत: Health Canada

इसे खरीदें

सक्रिय संघटक:

DICLOFENAC SODIUM

थमां उपलब्ध:

NOVARTIS PHARMACEUTICALS CANADA INC

ए.टी.सी कोड:

S01BC03

INN (इंटरनेशनल नाम):

DICLOFENAC

डोज़:

0.1%

फार्मास्यूटिकल फॉर्म:

SOLUTION

रचना:

DICLOFENAC SODIUM 0.1%

प्रशासन का मार्ग:

OPHTHALMIC

पैकेज में यूनिट:

0.3/2.5/5/10ML

प्रिस्क्रिप्शन प्रकार:

Prescription

चिकित्सीय क्षेत्र:

NONSTEROIDAL ANTI-INFLAMMATORY AGENTS

उत्पाद समीक्षा:

Active ingredient group (AIG) number: 0114417004; AHFS:

प्राधिकरण का दर्जा:

APPROVED

प्राधिकरण की तारीख:

2008-04-04

उत्पाद विशेषताएं

                                _VOLTAREN_
®
_ OPHTHA Diclofenac Sodium _
_Page 1 of 27_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
Pr
VOLTAREN® OPHTHA
Diclofenac Sodium Ophthalmic Solution
Ophthalmic solution, 0.1% w/v for Topical use
Anti-inflammatory agents, non-steroids
Novartis Pharmaceuticals Canada Inc.
700 Saint-Hubert St.,Suite 100
Montreal, Quebec
H2Y0C1
www.novartis.ca
Date of Initial Authorization:
SEPT 13, 1991
Date of Revision:
APR 11, 2023
Submission Control Number: 269518
VOLTAREN is a registered trademark.
_ _
_VOLTAREN_
®
_ OPHTHA Diclofenac Sodium _
_Page 2 of 27_
RECENT MAJOR LABEL CHANGES
7 WARNINGS AND PRECAUTIONS, Reproductive Health:
Female and Male Potential
04/2023
7 WARNINGS AND PRECAUTIONS, 7.1.1 Pregnant
Women
04/2023
SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF
AUTHORIZATION ARE NOT LISTED.
TABLE OF CONTENTS
RECENT MAJOR LABEL CHANGES
............................................................................................
2
TABLE OF CONTENTS
..............................................................................................................
2
PART I: HEALTH PROFESSIONAL INFORMATION
......................................................................
4
1
INDICATIONS
...............................................................................................................
4
1.1 Pediatrics
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4
1.2 Geriatrics
................................................................................................................
4
2
CONTRAINDICATIONS
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4
4
DOSAGE AND ADMINISTRATION
.................................................................................
4
4.2 Recommended Dose and Dosage Adjustment
....................................................... 4
4.4 Administration
........................................................................................
                                
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