ZYNQUISTA Film-coated tablet Ref.[10997] Active ingredients: Sotagliflozin

Source: European Medicines Agency (EU)  Revision Year: 2020  Publisher: Guidehouse Germany GmbH, Albrechtstr. 10c, 10117 Berlin, Germany

Product name and form

Zynquista 200 mg film-coated tablets.

Pharmaceutical Form

Film-coated tablet (tablet).

Oval, blue, film-coated tablet printed with “2456” on one side in black ink (tablet length: 14.2 mm, tablet width: 8.7 mm).

Qualitative and quantitative composition

Each tablet contains 200 mg sotagliflozin.

For the full list of excipients, see section 6.1.

Active Ingredient Description
Sotagliflozin

Sotagliflozin is an inhibitor of SGLT2 and SGLT1. Inhibiting SGLT2 reduces renal reabsorption of glucose and sodium which may influence several physiological functions such as lowering both pre-and afterload of the heart and downregulating sympathetic activity. Inhibiting SGLT1 reduces intestinal absorption of glucose and sodium which likely contributes to diarrhea. The mechanism for sotagliflozin’s cardiovascular benefits has not been established.

List of Excipients

Tablet core:

Microcrystalline cellulose (E460i)
Croscarmellose sodium
Colloidal anhydrous silica
Magnesium stearate
Talc

Film-coating:

Poly(vinyl alcohol)
Macrogol
Titanium dioxide (E171)
Talc
Indigo carmine aluminium lake (E132)

Printing ink:

Shellac
Iron oxide black (E172)
Propylene glycol

Pack sizes and marketing

PVC/PCTFE/Aluminium opaque blisters.

Pack sizes of 10, 20, 30, 60, 90, 100, 180 film-coated tablets, and a multipack of 200 film-coated tablets (2 packs of 100 film-coated tablets).

Not all pack sizes may be marketed.

Marketing authorization holder

Guidehouse Germany GmbH, Albrechtstr. 10c, 10117 Berlin, Germany

Marketing authorization dates and numbers

Zynquista 200 mg film coated tablets:

EU/1/19/1363/001 10 film coated tablets
EU/1/19/1363/002 20 film coated tablets
EU/1/19/1363/003 30 film coated tablets
EU/1/19/1363/004 60 film coated tablets
EU/1/19/1363/005 90 film coated tablets
EU/1/19/1363/006 100 film coated tablets
EU/1/19/1363/007 180 film coated tablets
EU/1/19/1363/008 200 (2x100) film coated tablets (multipack)

Date of first authorisation: 26 April 2019

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