PRIVA-VALACYCLOVIR TABLET

Country: Canada

Language: English

Source: Health Canada

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Active ingredient:

VALACYCLOVIR (VALACYCLOVIR HYDROCHLORIDE)

Available from:

PHARMAPAR INC

ATC code:

J05AB11

INN (International Name):

VALACICLOVIR

Dosage:

500MG

Pharmaceutical form:

TABLET

Composition:

VALACYCLOVIR (VALACYCLOVIR HYDROCHLORIDE) 500MG

Administration route:

ORAL

Units in package:

30/100

Prescription type:

Prescription

Therapeutic area:

NUCLEOSIDES AND NUCLEOTIDES

Product summary:

Active ingredient group (AIG) number: 0128626001; AHFS:

Authorization status:

CANCELLED POST MARKET

Authorization date:

2022-07-29

Summary of Product characteristics

                                _Priva-VALACYCLOVIR _
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PRODUCT MONOGRAPH
PR
PRIVA-VALACYCLOVIR
valacyclovir (as valacyclovir hydrochloride)
Valacyclovir Tablets 500 mg USP
Antiviral Agent
PHARMAPAR INC.
DATE OF PREPARATION:
100-5950, Ch. de la Côte de Liesse
June 3, 2015
Mont-Royal
QC H4T 1E2
Control#: 184603
_Priva-VALACYCLOVIR _
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_Page 2 of 39 _
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
.............................................................................
3
SUMMARY PRODUCT INFORMATION
.................................................................................................
3
INDICATIONS AND CLINICAL USE
.......................................................................................................
3
CONTRAINDICATIONS
............................................................................................................................
3
WARNINGS AND PRECAUTIONS
...........................................................................................................
4
ADVERSE REACTIONS
.............................................................................................................................
7
DRUG INTERACTIONS
...........................................................................................................................
13
DOSAGE AND ADMINISTRATION
.......................................................................................................
14
OVERDOSAGE
.........................................................................................................................................
16
ACTION AND CLINICAL PHARMACOLOGY
.....................................................................................
16
STORAGE AND STABILITY
...................................................................................................................
18
DOSAGE FORMS, COMPOSITION AND PACKAGING
......................................................................
18
PART II: SCIENTIFIC INFORMATION
.........................................
                                
                                Read the complete document
                                
                            

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