ALTACE CAPSULE

Ülke: Kanada

Dil: İngilizce

Kaynak: Health Canada

şimdi satın al

Indir Ürün özellikleri (SPC)
08-01-2021

Aktif bileşen:

RAMIPRIL

Mevcut itibaren:

BAUSCH HEALTH, CANADA INC.

ATC kodu:

C09AA05

INN (International Adı):

RAMIPRIL

Doz:

10MG

Farmasötik formu:

CAPSULE

Kompozisyon:

RAMIPRIL 10MG

Uygulama yolu:

ORAL

Paketteki üniteler:

30/100/500

Reçete türü:

Prescription

Terapötik alanı:

ANGIOTENSIN-CONVERTING ENZYME INHIBITORS

Ürün özeti:

Active ingredient group (AIG) number: 0122858002; AHFS:

Yetkilendirme durumu:

APPROVED

Yetkilendirme tarihi:

1996-06-05

Ürün özellikleri

                                PRODUCT MONOGRAPH
PR
ALTACE
®
Ramipril Capsules, USP
Capsules 1.25 mg, 2.5 mg, 5.0 mg, 10.0 mg, and 15 mg
Ramipril Tablets, USP
Tablets 1.25 mg, 2.5 mg, 5.0 mg and 10.0 mg
ATC CODE: C09AA05
ANGIOTENSIN CONVERTING ENZYME INHIBITOR
BAUSCH HEALTH, CANADA INC.
DATE OF REVISION:
2150 St-Elzear Blvd. West
January 8, 2021
Laval, Quebec
H7L 4A8
Control #: 239641
_Pr_
_ALTACE_
_®_
_ Product Monograph _
_Page 2 of 42_
_ _
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
............................................................ 3
SUMMARY
PRODUCT
INFORMATION
..................................................................................
3
INDICATIONS
AND
CLINICAL
USE
........................................................................................
4
CONTRAINDICATIONS
.............................................................................................................
5
WARNINGS
AND
PRECAUTIONS
............................................................................................
6
ADVERSE
REACTIONS
............................................................................................................
13
DRUG
INTERACTIONS
............................................................................................................
18
DOSAGE
AND
ADMINISTRATION
........................................................................................
21
OVERDOSAGE
..........................................................................................................................
23
ACTION
AND
CLINICAL
PHARMACOLOGY
.......................................................................
24
STORAGE
AND
STABILITY
....................................................................................................
27
DOSAGE
FORMS,
COMPOSITION
AND
PACKAGING ........................................................ 27
PART II: SCIENTIFIC INFORMATION
..................................................................................
30
PHARMACEUTICAL
INFORMATION
................................
                                
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