FIELD: medicine. SUBSTANCE: claimed form is substantially free of any other physical forms, is crystalline and has powder X-ray pattern with characteristic maximums at 14.0, 19.0, 22.0, 22.4 and 24.7 °. Present invention describes methods of preparation of said form and pharmaceutical compositions containing it. The claimed compound is essentially agent which has antileucotriene activity and is useful for treating diseases such as asthma. EFFECT: improved properties of the pharmaceutical composition. 4 cl, 2 dwg, 1 tbl
Title |
Year |
Author |
Number |
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- Dzhejms Dzhozef Kholokhan[Gb]
- Ieuan Dzhon Ehdvrds[Gb]
- Robert Dzhozef Timko[Us]
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- Arlin Klements[Us]
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|
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|
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- Alan Dunkan Robertson[Gb]
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|
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