FIELD: medicine; pharmaceutics.
SUBSTANCE: invention relates to a method of producing tablets of N-butyl-N-methyl-1-phenylpyrrolo[1,2-a]pyrazine-3-carboxamide. Method of producing tabletted form of N-butyl-N-methyl-1-phenylpyrrolo[1,2-a]pyrazine-3-carboxamide by wet granulation, where N-butyl-N-methyl-1-phenylpyrrolo[1,2-a]pyrazine-3-carboxamide weighing 1 mg and polyvinylpyrrolidone weighing 15 mg are dissolved in 14–59 mg of an aqueous-alcoholic or alcohol solution containing 34–96 % ethyl alcohol, then the obtained solution is moistened with a mixture of pre-sieved auxiliary substances: lactose 45 mg, microcrystalline cellulose 30 mg, cross-linked polyvinylpyrrolidone 4 mg, croscarmellose sodium 4 mg, after which the obtained mixture is punched through a sieve with diameter of 2 mm using a granulator, dried in a drying cabinet at temperature of 40–65 °C for 8–12 hours, then repeatedly punched through a sieve, obtained granules are powdered with magnesium stearate 1 mg, followed by pressing into tablets weighing 100 mg.
EFFECT: disclosed is a method of producing tablets of N-butyl-N-methyl-1-phenylpyrrolo[1,2-a]pyrazine-3-carboxamide.
1 cl, 2 tbl, 4 ex
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Authors
Dates
2024-12-05—Published
2023-04-11—Filed