BOSENTAN TABLET

देश: कनाडा

भाषा: अंग्रेज़ी

स्रोत: Health Canada

इसे खरीदें

सक्रिय संघटक:

BOSENTAN (BOSENTAN MONOHYDRATE)

थमां उपलब्ध:

PANDA PHARMACEUTICALS INC.

ए.टी.सी कोड:

C02KX01

INN (इंटरनेशनल नाम):

BOSENTAN

डोज़:

62.5MG

फार्मास्यूटिकल फॉर्म:

TABLET

रचना:

BOSENTAN (BOSENTAN MONOHYDRATE) 62.5MG

प्रशासन का मार्ग:

ORAL

पैकेज में यूनिट:

30/60/100

प्रिस्क्रिप्शन प्रकार:

Prescription

चिकित्सीय क्षेत्र:

VASODILATING AGENTS

उत्पाद समीक्षा:

Active ingredient group (AIG) number: 0145922001; AHFS:

प्राधिकरण का दर्जा:

APPROVED

प्राधिकरण की तारीख:

2017-09-22

उत्पाद विशेषताएं

                                1
PRODUCT MONOGRAPH PR
BOSENTAN
62.5 mg and 125 mg Bosentan (as monohydrate)
(film coated) Tablet
Endothelin Receptor Antagonist
PANDA Pharmaceuticals Inc.
35 Nixon Road, Unit 10
Caledon, Ontario
L7E 1K1
Date of Preparation: SEPTEMBER 21, 2017
Submission Control No: 200531
2
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
......................................................... 3
SUMMARY PRODUCT INFORMATION
...............................................................................
3
INDICATIONS AND CLINICAL USE
.....................................................................................
3
CONTRAINDICATIONS
...........................................................................................................
3
WARNINGS AND PRECAUTIONS
.........................................................................................
4
ADVERSE REACTIONS
...........................................................................................................
8
DRUG INTERACTIONS
.........................................................................................................
15
DOSAGE AND ADMINISTRATION
.....................................................................................
18
OVERDOSAGE
........................................................................................................................
19
ACTION AND CLINICAL PHARMACOLOGY
....................................................................
19
STORAGE AND STABILITY
.................................................................................................
21
SPECIAL HANDLING INSTRUCTIONS
...............................................................................
21
DOSAGE FORMS, COMPOSITION AND PACKAGING
.................................................... 21
PART II: SCIENTIFIC INFORMATION
..............................................................................
23
PHARMACEUTICAL INFORMATION
.................................................................................
23
CLINICAL TRIAL
                                
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