WO2026146530 - ATORVASTATIN ORAL SUSPENSION WITH IMPROVED STABILITY AND A METHOD FOR THE PRODUCTION THEREOF

National phase entry is expected:
Publication Number WO/2026/146530
Publication Date 09.07.2026
International Application No. PCT/IN2025/052157
International Filing Date 29.12.2025
Title **
[English] ATORVASTATIN ORAL SUSPENSION WITH IMPROVED STABILITY AND A METHOD FOR THE PRODUCTION THEREOF
[French] SUSPENSION ORALE D'ATORVASTATINE À STABILITÉ AMÉLIORÉE ET UN DE SES PROCÉDÉS DE PRODUCTION
Applicants **
WOCKHARDT LIMITED
Inventors
SEETHARAMAN, Sritharan
MHASE, Sunil
JENA, Nitishkumar
DUBE, Amol
JAJJAR, Rajeshkumar
Priority Data
202421104453   30.12.2024   IN
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Quotation for National Phase entry

Country StagesTotal
China Filing, Examination, Granting1969
EPO Filing, Examination, Granting11440
Japan Filing, Examination, Granting2057
South Korea Filing, Examination, Granting1851
USA Filing, Examination, Granting4740
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Total: 22,057
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Abstract[English] A stable oral suspension composition of Atorvastatin comprising 0.41% w/v of Atorvastatin calcium trihydrate, 0.20% w/v of Carmellose sodium, 0.60% w/v of Magnesium aluminum silicate, 0.3% w/v of parabens, 0.30% w/v of Sucralose, 0.10% w/v of Acesulfame potassium, 0.30% w/v of Orange flavour and Water. A process for the preparation of said suspension composition is also disclosed.[French] L'invention concerne une composition de suspension orale stable d'atorvastatine comprenant 0,41 % p/v d'atorvastatine calcique trihydrate, 0,20 % p/v de carmellose sodique, 0,60 % p/v de silicate de magnésium et d'aluminium, 0,3 % p/v de parabènes, 0,30 % p/v de sucralose, 0,10 % p/v d'acésulfame potassium, 0,30 % p/v d'arôme orange et de l'eau. L'invention divulgue également un procédé de préparation de ladite composition de suspension.