ACT Esomeprazole
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Generic name
esomeprazole magnesium dihydrate
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Brand reference
Nexium®
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Strength
40 mg
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DIN
02423863
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Therapeutic class
H+, K+ - ATPase Inhibitor
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Therapeutic area
Gastrointestinal
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Package size
Bottle 100
Blister 30
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Product code
17561-1040
17561-1027
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UPC
830790006193
830790006216
-
Generic name:
esomeprazole magnesium dihydrate
-
Brand reference:
Nexium®
-
Product code:
17561-1040
17561-1027
-
Strength
40 mg
-
DIN
02423863
-
UPC:
830790006193
830790006216
-
Therapeutic class
H+, K+ - ATPase Inhibitor
-
Therapeutic area:
Gastrointestinal
-
Package size:
Bottle 100
Blister 30
Composition
Active ingredient
esomeprazole magnesium dihydrate
Non-medicinal ingredients
crospovidone, hypromellose, hydroxypropyl cellulose, glyceryl monostearate, macrogol, magnesium stearate, methacrylic acid ethyl acrylate copolymer, microcrystalline cellulose, polysorbate 80, povidone K30, sodium stearyl fumarate, sugar spheres, talc and triethyl citrate. Coating: hypromellose, iron oxide red, iron oxide yellow, macrogol and titanium dioxide. Imprint: iron oxide black, propylene glycol and shellac glaze
Product characteristics
-
Dosage form
tablet
-
Shape
elliptical, biconvex
-
Marking 1
A160
-
Marking 2
-
Colour
pink
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Secondary colour
-
Scored
-
Flavour
-
Gluten
currently not available
-
Latex
not applicable
Disclaimers
All information about raw materials and/or allergen information for Teva Canada’s products is obtained from our suppliers and/or third-party affiliates and is based on their records.
Please be advised that the Medical Information department is not always notified of change in third-party affiliates and/or change in suppliers of the active and inactive ingredients that may occur over time, and all information provided herein is based on our last records on file.
Our manufacturing sites are not certified gluten-free. Raw materials and finished products are not tested for the presence of gluten. Therefore, the presence of trace amounts of gluten in the raw materials and in the finished products cannot be excluded.
"Latex" refers to NATURAL RUBBER LATEX. We cannot guarantee that there is no latex in the outer packaging, or that the medication or packaging haven’t come into contact with latex at any point during the manufacturing process; however, this is very unlikely due to the strict GMP procedures that are in place in all of our manufacturing facilities. Employees in the manufacturing and/or packaging facilities may be wearing latex gloves.
Product monograph/consumer information leaflet
View monograph
Notice
We are modifying our product names to align with our corporate name change. Accordingly, please expect product monographs to contain the “Novo-”, “ratio-”, “ACT”, "CO" prefix or the new “Teva” prefix. These prefixes may be used interchangeably on the website.
Should you have any questions about our product names or our corporate name change, please do not hesitate to contact us. Our Customer Care department can be reached at 1-800-268-4127 regarding your inquiry.