OMEPRAZOLE CAPSULE (DELAYED RELEASE)

Šalis: Kanada

kalba: anglų

Šaltinis: Health Canada

Nusipirk tai dabar

Parsisiųsti Prekės savybės (SPC)
13-10-2023

Veiklioji medžiaga:

OMEPRAZOLE

Prieinama:

PRO DOC LIMITEE

ATC kodas:

A02BC01

INN (Tarptautinis Pavadinimas):

OMEPRAZOLE

Dozė:

20MG

Vaisto forma:

CAPSULE (DELAYED RELEASE)

Sudėtis:

OMEPRAZOLE 20MG

Vartojimo būdas:

ORAL

Vienetai pakuotėje:

100/500

Recepto tipas:

Prescription

Gydymo sritis:

PROTON-PUMP INHIBITORS

Produkto santrauka:

Active ingredient group (AIG) number: 0121643001; AHFS:

Autorizacija statusas:

APPROVED

Leidimo data:

2010-02-05

Prekės savybės

                                _OMEPRAZOLE (Omeprazole delayed-release capsules) _
_Page 1 of 49 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
OMEPRAZOLE
Omeprazole Delayed-Release Capsules
Capsules (delayed release), 20 mg, Oral
Manufacturer’s Standard
Proton Pump Inhibitor
PRO DOC LTÉE
2925 boul. Industriel
Laval, Québec
H7L 3W9
Submission Control Number: 279464
Date of Initial Authorization:
FEB 05, 2010
Date of Revision:
OCT 13, 2023
_OMEPRAZOLE (Omeprazole delayed-release capsules) _
_Page 2 of 49 _
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
....................................................... 5
4.4
Administration
.........................................................................................................
7
4.5
Missed Dose
...........................................
                                
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