AURO-ONDANSETRON ODT TABLET (ORALLY DISINTEGRATING)

Pajjiż: Kanada

Lingwa: Ingliż

Sors: Health Canada

Ixtrih issa

Ingredjent attiv:

ONDANSETRON

Disponibbli minn:

AURO PHARMA INC

Kodiċi ATC:

A04AA01

INN (Isem Internazzjonali):

ONDANSETRON

Dożaġġ:

8MG

Għamla farmaċewtika:

TABLET (ORALLY DISINTEGRATING)

Kompożizzjoni:

ONDANSETRON 8MG

Rotta amministrattiva:

ORAL

Unitajiet fil-pakkett:

15G/50G

Tip ta 'preskrizzjoni:

Prescription

Żona terapewtika:

5-HT3 RECEPTOR ANTAGONISTS

Sommarju tal-prodott:

Active ingredient group (AIG) number: 0131120001; AHFS:

L-istatus ta 'awtorizzazzjoni:

APPROVED

Data ta 'l-awtorizzazzjoni:

2021-01-20

Karatteristiċi tal-prodott

                                Page 1 of 35
_PRODUCT MONOGRAPH _
_AURO-ONDANSETRON ODT_
_ _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
AURO-ONDANSETRON ODT
Ondansetron Orally Disintegrating Tablets
Orally Disintegrating Tablets, 4 mg and 8 mg, Oral
House Standard
Antiemetic
5-HT
3
receptor antagonist
ATC code A04AA01
Auro Pharma Inc.
3700 Steeles Avenue West, Suite # 402
Woodbridge, Ontario, L4L 8K8, Canada.
Date of Initial Authorization:
January 20, 2021
Date of Revision:
September 08, 2022
Submission Control Number: 261680
Page 2 of 35
_PRODUCT MONOGRAPH _
_AURO-ONDANSETRON ODT_
_ _
RECENT MAJOR LABEL CHANGES
1 INDICATIONS, Adults (18-64 years of age)
09/2022
4 DOSAGE AND ADMINISTRATION, 4.2 Recommended Dose and Dose Adjustment
09/2022
7 WARNINGS AND PRECAUTIONS, Cardiovascular, Myocardial Ischemia and
Coronary Artery Spasm
09/2022
7 WARNINGS AND PRECAUTIONS, Special Populations, 7.1.1 Pregnant Women
01/2021
TABLE OF CONTENTS
SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF
AUTHORIZATION ARE NOT LISTED.
RECENT MAJOR LABEL CHANGES
..........................................................................................
2
PART I: HEALTH PROFESSIONAL INFORMATION
.................................................................... 4
1 INDICATIONS
....................................................................................................................
4
1.1 Pediatrics (<18 years of age)
.......................................................................................
4
1.2 Geriatrics (≥65 years of age)
.......................................................................................
4
2 CONTRAINDICATIONS
.......................................................................................................
4
4 DOSAGE AND ADMINISTRATION
.......................................................................................
5
4.1 Dosing Considerations
................................................................................................
5
4.2 Recommended Dose and Dosage Adjustment
                                
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