Source: European Medicines Agency (EU) Revision Year: 2026 Publisher: Aziende Chimiche Riunite Angelini Francesco – A.C.R.A.F. S.p.A., Viale Amelia 70, 00181, Rome - Italy
Latuda 18.5 mg film-coated tablets.
Latuda 37 mg film-coated tablets.
Latuda 74 mg film-coated tablets.
| Pharmaceutical Form |
|---|
|
Film-coated tablet (tablet). Latuda 18.5 mg film-coated tablets: White to off-white, film-coated round tablets of 6 mm debossed with 'LA'. Latuda 37 mg film-coated tablets: White to off-white, film-coated round tablets of 8 mm debossed with 'LB'. Latuda 74 mg film-coated tablets: Pale green, film-coated oval tablets of 12 mm x 7 mm debossed with 'LD. |
Latuda 18.5 mg film-coated tablets: Each film-coated tablet contains lurasidone hydrochloride equivalent to18.6 mg lurasidone.
Latuda 37 mg film-coated tablets: Each film-coated tablet contains lurasidone hydrochloride equivalent to 37.2 mg lurasidone.
Latuda 74 mg film-coated tablets: Each film-coated tablet contains lurasidone hydrochloride equivalent to 74.5 mg lurasidone.
For the full list of excipients, see section 6.1.
| Active Ingredient |
|---|
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Lurasidone is a selective blocking agent of dopamine and monoamine effects indicated for the treatment of schizophrenia. Lurasidone binds strongly to dopaminergic D2- and to serotonergic 5-HT2A and 5-HT7 receptors. Lurasidone does not bind to histaminergic or muscarinic receptors. |
| List of Excipients |
|---|
Latuda 18.5 mg film-coated tabletsCore: Mannitol (E421) Tablet coating: Hypromellose 2910 (E464) Latuda 37 mg film-coated tabletsCore: Mannitol (E421) Tablet coating: Hypromellose 2910 (E464) Latuda 74 mg film-coated tabletsCore: Mannitol (E421) Tablet coating: Hypromellose 2910 (E464) |
Cartons contain 14 x 1, 28 x 1, 30 x 1, 56 x 1, 60 x 1, 90 x 1 or 98 x 1 tablets in aluminium/aluminium perforated unit dose blisters.
Not all pack sizes may be marketed.
Aziende Chimiche Riunite Angelini Francesco – A.C.R.A.F. S.p.A., Viale Amelia 70, 00181, Rome - Italy
Latuda 18.5 mg film-coated tablet: EU/1/14/913/001-007
Latuda 37 mg film-coated tablet: EU/1/14/913/008-014
Latuda 74 mg film-coated tablet: EU/1/14/913/015-021
Date of first authorisation: 21 March 2014
Date of latest renewal: 14 November 2018
| Drug | Countries | |
|---|---|---|
| LATUDA | Austria, Australia, Brazil, Canada, Estonia, Spain, Finland, Hong Kong, Croatia, Ireland, Italy, Japan, Lithuania, Netherlands, Poland, Romania, Singapore, United Kingdom, United States |
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