Oral medicine composition for treating obesity or vascular hypertension
A technology for hypertension and composition, applied in the field of medicine, can solve problems such as no reports, and achieve the effects of simple production process, reduced incidence, and reduced drug side effects
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Embodiment 1
[0019] Embodiment 1: Prescription of compound orlistat / nifedipine tablet (1000 tablets)
[0020]
[0021]
[0022] Preparation Process:
[0023] (1) Granulation After orlistat, nifedipine, and lactose were sieved and mixed with 80 meshes, they were put into the mixing system together with hydroxypropyl methylcellulose, cross-linked carmellose sodium, and microcrystalline cellulose. Granulator, mixed, evenly added 5% PVP85% ethanol solution for wet granulation, took out the granules and carried out wet granulation with a 20-mesh sieve, after drying, passed through a 20-mesh sieve for granulation, and set aside.
[0024] (2) Compression: Mix the prepared granules with the prescribed amount of magnesium stearate evenly, and compress into tablets to obtain final product.
Embodiment 2
[0025] Embodiment 2: Prescription of compound orlistat / nifedipine tablet (1000 tablets)
[0026]
[0027] Preparation Process:
[0028] (1) Granulation After orlistat, nifedipine, and lactose were sieved and mixed with 80 meshes, they were put into the mixing system together with hydroxypropyl methylcellulose, cross-linked carmellose sodium, and microcrystalline cellulose. Granulator, mixed, evenly added 5% PVP85% ethanol solution for wet granulation, took out the granules and carried out wet granulation with a 20-mesh sieve, after drying, passed through a 20-mesh sieve for granulation, and set aside.
[0029] (2) Compression: Mix the prepared granules with the prescribed amount of magnesium stearate evenly, and compress into tablets to obtain final product.
Embodiment 3
[0030] Embodiment 3: Prescription of compound orlistat / nifedipine tablet (1000 tablets)
[0031]
[0032]
[0033] Preparation Process:
[0034] (1) Granulation After orlistat, nifedipine, and lactose were sieved and mixed with 80 meshes, they were put into the mixing system together with hydroxypropyl methylcellulose, cross-linked carmellose sodium, and microcrystalline cellulose. Granulator, mixed, evenly added 5% PVP85% ethanol solution for wet granulation, took out the granules and carried out wet granulation with a 20-mesh sieve, after drying, passed through a 20-mesh sieve for granulation, and set aside.
[0035] (3) Compression: mix the prepared granules with the prescribed amount of magnesium stearate, and then compress into tablets to obtain final product.
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