PYRIDIUM TABLET

Land: Canada

Språk: engelsk

Kilde: Health Canada

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Last ned Preparatomtale (SPC)
24-10-2022

Aktiv ingrediens:

PHENAZOPYRIDINE HYDROCHLORIDE

Tilgjengelig fra:

SEARCHLIGHT PHARMA INC

ATC-kode:

G04BX06

INN (International Name):

PHENAZOPYRIDINE

Dosering :

200MG

Legemiddelform:

TABLET

Sammensetning:

PHENAZOPYRIDINE HYDROCHLORIDE 200MG

Administreringsrute:

ORAL

Enheter i pakken:

250ML

Resept typen:

Prescription

Terapeutisk område:

ANTIPRURITICS AND LOCAL ANESTHETICS

Produkt oppsummering:

Active ingredient group (AIG) number: 0106949002; AHFS:

Autorisasjon status:

APPROVED

Autorisasjon dato:

2005-07-08

Preparatomtale

                                PRESCRIBING INFORMATION
Pr
PYRIDIUM
Phenazopyridine Hydrochloride Tablets USP
100 mg and 200 mg
Urinary Tract Analgesic
Date of Preparation:
OCT 24, 2022
Searchlight Pharma Inc.
1600 Notre-Dame West, Suite 312
Montreal, Quebec
H3J 1M1
Submission Control No.: 267654
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PYRIDIUM
®
(Phenazopyridine Hydrochloride) – Prescribing information Page 2 of
16
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
.................................... 3
SUMMARY PRODUCT INFORMATION
.................................................... 3
INDICATIONS AND CLINICAL USE
.......................................................... 3
CONTRAINDICATIONS
...............................................................................
4
WARNINGS AND PRECAUTIONS
.............................................................. 4
ADVERSE REACTIONS
................................................................................
6
DRUG INTERACTIONS
................................................................................
7
DOSAGE AND ADMINISTRATION
............................................................ 7
OVERDOSAGE...............................................................................................
8
ACTION AND CLINICAL PHARMACOLOGY
.......................................... 8
STORAGE AND STABILITY
........................................................................
9
DOSAGE FORMS, COMPOSITION AND PACKAGING ........................... 9
PART II: SCIENTIFIC INFORMATION
.......................................................... 10
PHARMACEUTICAL
INFORMATION...................................................... 10
DETAILED PHARMACOLOGY
................................................................. 10
TOXICOLOGY
.............................................................................................
10
REFERENCES...............................................................................................
12
PART III: CONSUMER INFORMATION
......................................................... 13
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