AG-METOPROLOL-L TABLET

País: Canadà

Idioma: anglès

Font: Health Canada

ingredients actius:

METOPROLOL TARTRATE

Disponible des:

ANGITA PHARMA INC.

Codi ATC:

C07AB02

Designació comuna internacional (DCI):

METOPROLOL

Dosis:

50MG

formulario farmacéutico:

TABLET

Composición:

METOPROLOL TARTRATE 50MG

Vía de administración:

ORAL

Unidades en paquete:

100/500

tipo de receta:

Prescription

Área terapéutica:

BETA-ADRENERGIC BLOCKING AGENTS

Resumen del producto:

Active ingredient group (AIG) number: 0111923002; AHFS:

Estat d'Autorització:

APPROVED

Data d'autorització:

2018-10-02

Fitxa tècnica

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PRODUCTMONOGRAPH
PR
AG-METOPROLOL-L
Metoprolol Tartrate Tablets USP
25mg, 50 mg and 100 mg film coated tablets,
USP
β-Adrenergic Receptor Blocking Agent
Angita Pharma Inc
1310 rue Nobel
Boucherville, Québec
J4B 5H3, Canada
Submission Control No: 266208
Date
of
Revision:
August 10, 2022
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TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
.......................................................... 3
SUMMARY PRODUCT
INFORMATION
..........................................................................
3
INDICATIONS AND CLINICAL USE
...............................................................................
3
CONTRAINDICATIONS
....................................................................................................
4
WARNINGS AND
PRECAUTIONS
....................................................................................
5
ADVERSE REACTIONS
..................................................................................................
10
DRUG INTERACTIONS
..................................................................................................
12
DOSAGE AND ADMINISTRATION
...............................................................................
18
OVERDOSAGE
.................................................................................................................
20
ACTION AND CLINICAL PHARMACOLOGY
............................................................. 21
STORAGE AND STABILITY
..........................................................................................
24
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................. 25
PART II: SCIENTIFIC
INFORMATION ..................................................................................
26
PHARMACEUTICAL INFORMATION
..........................................................................
26
CLINICAL TRIALS
...................................................................