AG-MOXIFLOXACIN TABLET

Riik: Kanada

keel: inglise

Allikas: Health Canada

Toimeaine:

MOXIFLOXACIN (MOXIFLOXACIN HYDROCHLORIDE)

Saadav alates:

ANGITA PHARMA INC.

ATC kood:

J01MA14

INN (Rahvusvaheline Nimetus):

MOXIFLOXACIN

Annus:

400MG

Ravimvorm:

TABLET

Koostis:

MOXIFLOXACIN (MOXIFLOXACIN HYDROCHLORIDE) 400MG

Manustamisviis:

ORAL

Ühikuid pakis:

30

Retsepti tüüp:

Prescription

Terapeutiline ala:

QUINOLONES

Toote kokkuvõte:

Active ingredient group (AIG) number: 0142242001; AHFS:

Volitamisolek:

APPROVED

Loa andmise kuupäev:

2018-06-28

Toote omadused

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_MOXIFLOXACIN _
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PRODUCT MONOGRAPH
PR
AG
-
MOXIFLOXACIN
Moxifloxacin Tablets
400 mg
(as moxifloxacin hydrochloride)
Antibacterial Agent
Date
of
Revision:
August 03, 2022
Manufactured
by:
Angita
Pharma
Inc.
1310 rue Nobel
Boucherville,Québec
J4B
5H3
Canada
SUBMISSION
CONTROL
NO:
265857
_AG-_
_MOXIFLOXACIN _
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TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
...........................................................
3
SUMMARY PRODUCT INFORMATION
.........................................................................
3
INDICATIONS AND CLINICAL USE
................................................................................
3
CONTRAINDICATIONS
....................................................................................................
5
WARNINGS AND PRECAUTIONS
...................................................................................
6
ADVERSE REACTIONS
..................................................................................................
14
DRUG INTERACTIONS
...................................................................................................
18
DOSAGE AND ADMINISTRATION
...............................................................................
20
OVERDOSAGE
.................................................................................................................
21
ACTION AND CLINICAL PHARMACOLOGY
.............................................................. 22
STORAGE AND STABILITY
...........................................................................................
29
SPECIAL HANDLING INSTRUCTIONS
.........................................................................
30
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................. 31
PART II: SCIENTIFIC INFORMATION
.................................................................................
32
PHARMACEUTICAL
INFORMATION
............................................................................
32
CLINICAL TRIALS
...