Estalis Continuous

国家: 新西兰

语言: 英文

来源: Medsafe (Medicines Safety Authority)

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下载 产品特点 (SPC)
13-12-2007

有效成分:

Estradiol hemihydrate 0.256mg equivalent to estradiol 25 µg/24 hours;  ; Norethisterone acetate 2.4mg equivalent to norethisterone acetate 125 µg/24 hours;  

可用日期:

Novartis New Zealand Ltd

INN(国际名称):

Estradiol hemihydrate 0.256 mg (equivalent to estradiol 25 µg/24 hours)

剂量:

25/125

药物剂型:

Transdermal patch

组成:

Active: Estradiol hemihydrate 0.256mg equivalent to estradiol 25 µg/24 hours   Norethisterone acetate 2.4mg equivalent to norethisterone acetate 125 µg/24 hours   Excipient: Acrylic adhesive Dipropylene glycol Oleic acid Povidone Silicone adhesive

每包单位数:

Sachet, aluminium foil, composite laminate: paper/low-density polyethylene/Al foil/coextrusion polyethylene, 8 patches

类:

Prescription

处方类型:

Prescription

厂商:

NV Organon

產品總結:

Package - Contents - Shelf Life: Sachet, aluminium foil, composite laminate: paper/low-density polyethylene/Al foil/coextrusion polyethylene - 8 patches - 24 months from date of manufacture stored at 2° to 8°C (Refrigerate, do not freeze) 6 months unopened stored at or below 25°C

授权日期:

2003-08-14

产品特点

                                 
1
NEW ZEALAND DATA SHEET 
 
ESTALIS
®
 CONTINUOUS 
(OESTRADIOL/NORETHISTERONE ACETATE) 
 
TRANSDERMAL PATCH RELEASING 
 
50 micrograms/24 hours of oestradiol and 140 micrograms/24 hours of
norethisterone acetate 
50 micrograms/24 hours of oestradiol and 250 micrograms/24 hours of
norethisterone acetate 
 
TRADE NAME(S) 
ESTALIS
®
 Continuous 50/140 
ESTALIS
®
 Continuous 50/250 
DESCRIPTION AND COMPOSITION 
PHARMACEUTICAL FORM 
Transdermal patch. 
ACTIVE SUBSTANCE(S) 
The active components of the Estalis
®
 Continuous matrix transdermal patch are oestradiol 
hemihydrate and norethisterone acetate. The remaining components
are pharmacologically 
inactive. 
Two Estalis Continuous matrix transdermal patches are available. They
release oestradiol 
and norethisterone acetate (NETA) in the following quantities and
at the following rates over a 
period of 3.5 to 4 days: 
NAME 
NOMINAL RELEASE RATE 
(MICROGRAM/DAY) 
OESTRADIOL/NETA 
OESTRADI
OL 
CONTENT 
(MG)* 
NETA 
CONTENT (MG)
SURFACE 
AREA (CM
2
) 
SHAPE 
Estalis 
Continuous 
50/140 0.620 
2.70 9 
Round 
Estalis 
Continuous 
50/250 0.512 
4.80 16 
Round 
*
 
1 mg oestradiol  hemihydrate is equivalent to 0.968 mg oestradiol 
 
_LIST OF EXCIPIENTS _
Adhesive matrix: silicone adhesive, acrylic adhesive, povidone, oleic
acid, dipropylene glycol, 
Backing layer: polyester film laminate, 
 
2
Protective (release liner): fluoropolymer coated polyester film. 
INDICATIONS 
The Estalis Continuous regimen is indicated for the following: 
•  Treatment of symptoms of oestrogen deficiency in
postmenopausal women with an intact 
uterus. 
•  Prevention of osteoporosis in postmenopausal women with an
intact uterus. (see sections 
Dosage and Administration and Warnings and Precautions). 
DOSAGE AND ADMINISTRATION 
DOSAGE 
ADULTS AND ELDERLY 
For all therapeutic indications, the lowest effective dose should be
used. 
Hormone replacement therapy (HRT) involving combined
oes
                                
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