PAIN RELIEVER & SLEEP AID TABLET

Land: Kanada

Språk: engelska

Källa: Health Canada

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Produktens egenskaper Produktens egenskaper (SPC)
30-09-2020

Aktiva substanser:

DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM

Tillgänglig från:

APOTEX INC

ATC-kod:

M01AE57

INN (International namn):

NAPROXEN AND DIPHENHYDRAMINE

Dos:

25MG; 220MG

Läkemedelsform:

TABLET

Sammansättning:

DIPHENHYDRAMINE HYDROCHLORIDE 25MG; NAPROXEN SODIUM 220MG

Administreringssätt:

ORAL

Enheter i paketet:

100

Receptbelagda typ:

OTC

Terapiområde:

OTHER NONSTEROIDAL ANTIIMFLAMMATORY AGENTS

Produktsammanfattning:

Active ingredient group (AIG) number: 0257270001; AHFS:

Bemyndigande status:

APPROVED

Tillstånd datum:

2020-10-08

Produktens egenskaper

                                Page 1 of 47
PRODUCT MONOGRAPH
PAIN RELIEVER & SLEEP AID
Naproxen Sodium 220 mg and Diphenhydramine Hydrochloride 25mg Tablets
Apotex Inc.
150 Signet Drive
Toronto, Ontario
Canada M9L 1T9
Date of Preparation:
September 30, 2020
Control No. 230683
Page 2 of 47
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
.......................................................................
3
SUMMARY PRODUCT INFORMATION
.................................................................................................
3
CONTRAINDICATIONS
............................................................................................................................
3
WARNINGS AND PRECAUTIONS
...........................................................................................................
4
ADVERSE REACTIONS
.............................................................................................................................
7
DRUG INTERACTIONS
...........................................................................................................................
12
DOSAGE AND ADMINISTRATION
.......................................................................................................
14
OVERDOSAGE...........................................................................................................................................
15
ACTION AND CLINICAL
PHARMACOLOGY......................................................................................
15
STORAGE AND STABILITY
...................................................................................................................
18
SPECIAL HANDLING INSTRUCTIONS
................................................................................................
18
DOSAGE FORMS, COMPOSITION AND PACKAGING
......................................................................
18
PART II: SCIENTIFIC INFORMATION
.............................................................................................
20
PHARMACEUTICAL INFORMATION
........
                                
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