TARO-IMIPENEM-CILASTATIN POWDER FOR SOLUTION

Land: Canada

Taal: Engels

Bron: Health Canada

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Productkenmerken Productkenmerken (SPC)
22-07-2022

Werkstoffen:

IMIPENEM; CILASTATIN (CILASTATIN SODIUM)

Beschikbaar vanaf:

SUN PHARMA CANADA INC

ATC-code:

J01DH51

INN (Algemene Internationale Benaming):

IMIPENEM AND CILASTATIN

Dosering:

500MG; 500MG

farmaceutische vorm:

POWDER FOR SOLUTION

Samenstelling:

IMIPENEM 500MG; CILASTATIN (CILASTATIN SODIUM) 500MG

Toedieningsweg:

INTRAVENOUS

Eenheden in pakket:

30ML

Prescription-type:

Prescription

Therapeutisch gebied:

CARBAPENEMS

Product samenvatting:

Active ingredient group (AIG) number: 0218820001; AHFS:

Autorisatie-status:

APPROVED

Autorisatie datum:

2021-01-19

Productkenmerken

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_TARO-Imipenem-Cilastatin (Imipenem and Cilastatin for Injection, USP)
Page 1 of 57 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
TARO-IMIPENEM-CILASTATIN
Imipenem and Cilastatin for Injection
250 mg imipenem and 250 mg cilastatin (as cilastatin sodium) per vial
500 mg imipenem and 500 mg cilastatin (as cilastatin sodium) per vial
Sterile powder for solution, I.V. Infusion
USP
ANTIBIOTIC
Sun Pharma Canada Inc.,
126 East Drive
Brampton, ON
L6T 1C1
Date of Initial Authorization:
MAY 20, 2010
Date of Revision:
JULY 22, 2022
Submission Control Number: 260927
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_TARO-Imipenem-Cilastatin (Imipenem and Cilastatin for Injection, USP)
Page 2 of 57 _
RECENT MAJOR LABEL CHANGES
4. DOSAGE AND ADMINISTRATION
07/2022
7. WARNINGS AND PRECAUTIONS
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
TABLE OF CONTENTS
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2
PART I: HEALTH PROFESSIONAL INFORMATION
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4
1
INDICATIONS........................................................................................................................
4
1.1 PEDIATRICS
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5
1.2 GERIATRICS
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5
2 CONTRAINDICATIONS
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5
3 SERIOUS WARNINGS AND PRECAUTIONS
BOX......................................................................
5
4 DOSAGE AND ADMINISTRATION
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6
4.
                                
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