RU2003136045A - MEDICINAL FORM, POSSESSING ANTI-ANGINAL ACTION, AND METHOD FOR PRODUCING IT - Google Patents

MEDICINAL FORM, POSSESSING ANTI-ANGINAL ACTION, AND METHOD FOR PRODUCING IT Download PDF

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Publication number
RU2003136045A
RU2003136045A RU2003136045/15A RU2003136045A RU2003136045A RU 2003136045 A RU2003136045 A RU 2003136045A RU 2003136045/15 A RU2003136045/15 A RU 2003136045/15A RU 2003136045 A RU2003136045 A RU 2003136045A RU 2003136045 A RU2003136045 A RU 2003136045A
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RU
Russia
Prior art keywords
stearic acid
starch
magnesium stearic
croscarmellose
dosage form
Prior art date
Application number
RU2003136045/15A
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Russian (ru)
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RU2260431C2 (en
Original Assignee
Закрытое акционерное общество "Фармацевтическое предпри тие "Оболенское" ( RU)
Закрытое акционерное общество "Фармацевтическое предприятие "Оболенское" ( RU)
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Application filed by Закрытое акционерное общество "Фармацевтическое предпри тие "Оболенское" ( RU), Закрытое акционерное общество "Фармацевтическое предприятие "Оболенское" ( RU) filed Critical Закрытое акционерное общество "Фармацевтическое предпри тие "Оболенское" ( RU)
Priority to RU2003136045/15A priority Critical patent/RU2260431C2/en
Publication of RU2003136045A publication Critical patent/RU2003136045A/en
Application granted granted Critical
Publication of RU2260431C2 publication Critical patent/RU2260431C2/en

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Claims (3)

1. Лекарственная форма, обладающая антиангинальным действием, состоящая из ядра, содержащего в качестве активного действующего начала триметадизидина дигидрохлорид и в качестве вспомогательных веществ магний стеариновокислый, и растворяющейся в желудке оболочки, отличающаяся тем, что ядро дополнительно содержит в качестве вспомогательных веществ крахмал, манит, повидон, кроскармелозу и микрокристаллическую целлюлозу при следующем соотношении компонентов, мас.%:1. A dosage form having antianginal action, consisting of a core containing, as an active active principle, trimethadisidine dihydrochloride and excipients, magnesium stearic acid, and a membrane that dissolves in the stomach, characterized in that the core additionally contains starch as an excipient, beckons, povidone, croscarmellose and microcrystalline cellulose in the following ratio of components, wt.%: Триметазидина дигидрохлорид 5,0-42,0Trimetazidine dihydrochloride 5.0-42.0 Крахмал 16,0-29,0Starch 16.0-29.0 Маннит 12,0-17,0Mannitol 12.0-17.0 Повидон 5,0-9,5Povidone 5.0-9.5 Магний стеариновокислый 0,5-1,5Magnesium stearic acid 0.5-1.5 Кроскармелоза 1,5-5,0Croscarmellose 1.5-5.0 Микрокристаллическая целлюлоза 23,0-33,0Microcrystalline cellulose 23.0-33.0 а оболочка содержит следующие компоненты, мас.%:and the shell contains the following components, wt.%: Оксипропилметилцеллюлоза 57,0-82,0Oxypropyl methylcellulose 57.0-82.0 Полиэтиленгликоль 5,0-10,0Polyethylene glycol 5.0-10.0 Двуокись титана 10,0-25,0Titanium dioxide 10.0-25.0 Магний стеариновокислый 1,0-3,0Magnesium stearic acid 1.0-3.0 Краситель кислотный красный 2с 2,0-5,0.Acid red dye 2s 2.0-5.0. 2. Лекарственная форма по п.1, отличающаяся тем, что в качестве крахмала содержит кукурузный крахмал.2. The dosage form according to claim 1, characterized in that the starch contains corn starch. 3. Способ изготовления лекарственной формы в соответствии с любым из пп.1 и 2, отличающийся тем, что смешивают триметадизидина дигидрохлорид, маннит, крахмал и микрокристаллическую целлюлозу, полученную смесь, увлажняют раствором повидона, повторно перемешивают, проводят влажную грануляцию, последующую сушку, сухую грануляцию, опудривание смесью кроскармелозы и магния стеариновокислого с последующим таблетированием и нанесением оболочки из водной суспензии, содержащей оксипропилметилцеллюлозу, полиэтиленгликоль, двуокись титана, магний стеариновокислый и краситель.3. A method of manufacturing a dosage form in accordance with any of claims 1 and 2, characterized in that trimethadisidine dihydrochloride, mannitol, starch and microcrystalline cellulose are mixed, the resulting mixture is moistened with povidone solution, re-mixed, wet granulation is carried out, followed by drying, dry granulation, dusting with a mixture of croscarmellose and magnesium stearic acid, followed by tabletting and coating from an aqueous suspension containing hydroxypropyl methylcellulose, polyethylene glycol, titanium dioxide, magnesium stearic acid and dye.
RU2003136045/15A 2003-12-15 2003-12-15 Medicinal formulation eliciting anti-anginal effect and method for its preparing RU2260431C2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
RU2003136045/15A RU2260431C2 (en) 2003-12-15 2003-12-15 Medicinal formulation eliciting anti-anginal effect and method for its preparing

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
RU2003136045/15A RU2260431C2 (en) 2003-12-15 2003-12-15 Medicinal formulation eliciting anti-anginal effect and method for its preparing

Publications (2)

Publication Number Publication Date
RU2003136045A true RU2003136045A (en) 2005-05-27
RU2260431C2 RU2260431C2 (en) 2005-09-20

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Family Applications (1)

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RU2003136045/15A RU2260431C2 (en) 2003-12-15 2003-12-15 Medicinal formulation eliciting anti-anginal effect and method for its preparing

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RU (1) RU2260431C2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA009810B1 (en) * 2006-12-26 2008-04-28 Закрытое Акционерное Общество "Канонфарма Продакшн" Matrix for manufacturing tableted dosage form and method of treatment

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RU2260431C2 (en) 2005-09-20

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PC4A Invention patent assignment

Effective date: 20071129

MM4A The patent is invalid due to non-payment of fees

Effective date: 20071216

NF4A Reinstatement of patent

Effective date: 20081227

PC4A Invention patent assignment

Effective date: 20100406

MM4A The patent is invalid due to non-payment of fees

Effective date: 20101216