Oral disintegration tablet of Amlodipine mesylate, and preparation method
A technology of amlodipine mesylate and orally disintegrating tablets, which is applied to pharmaceutical formulas, medical preparations containing active ingredients, pill delivery, etc., to achieve the effect of easy packaging, carrying and taking
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Embodiment 1
[0028] The formulation of the present invention consists of the following components by weight percentage:
[0029] Amlodipine mesylate 5.0g
[0030] Microcrystalline Cellulose 50.0g
[0031] Mannitol 100.0g
[0032] Cross-linked polyvinylpyrrolidone 9.0g
[0033] Sodium bicarbonate 4.0g
[0034] Citric acid 4.0g
[0035] Aspartame 1.5g
[0036] Mint essence 0.56g
[0037] Orange flavor 1.0g
[0038] Micronized silica gel 2.0g
[0039] Magnesium Stearate 1.0g
[0040] A total of 1000 pieces were made
[0041] The dosage form is prepared by direct compression technology using conventional tablet pharmaceutical equipment. The specific preparation method is as follows: Amlodipine mesylate, microcrystalline cellulose, mannitol, cross-linked polyvinylpyrrolidone, sodium bicarbonate, citric acid, aspartame, peppermint essence, orange essence are respectively Weigh, pass through an 80-mesh sieve and mix evenly; then mix with magnesium stearate and micropowder silica gel, s...
Embodiment 2
[0043] The formulation of the present invention consists of the following components by weight percentage:
[0044] Amlodipine mesylate 5.0g
[0045] Fast flowing lactose (Flowlac ) 150.0g
[0046] Croscarmellose Sodium 9.0g
[0047] Aspartame 1.8g
[0048] Mint essence 0.5g
[0049] Magnesium Stearate 1.0g
[0050] A total of 1000 pieces were made
[0051] The dosage form is prepared by direct compression technology using conventional tablet pharmaceutical equipment. The specific preparation method is as follows: amlodipine mesylate, fast flow lactose (Flowlac ), croscarmellose sodium, aspartame and peppermint essence were weighed respectively according to the amount, passed through an 80 mesh sieve and mixed evenly; then mixed with magnesium stearate, sieved and mixed evenly, and then the intermediate was carried out For content determination, directly compress the tablet according to the specified amount to obtain an orally disintegrating tablet.
Embodiment 3
[0053] The formulation of the present invention consists of the following components by weight percentage:
[0054] Amlodipine mesylate 5.0g
[0055] Microcrystalline Cellulose 80.0g
[0056] Mannitol 88.0g
[0057] Aspartame 1.8g
[0058] Mint essence 0.5g
[0059] Orange flavor 1.0g
[0060] Micronized silica gel 2.0g
[0061] Magnesium Stearate 1.0g
[0062] A total of 1000 pieces were made
[0063] The dosage form is prepared by direct compression technology using conventional tablet pharmaceutical equipment. The specific preparation method is as follows: Weigh amlodipine mesylate, microcrystalline cellulose, mannitol, aspartame, peppermint flavor, and orange flavor respectively according to the amount, pass through an 80-mesh sieve and mix evenly; Magnesium fatty acid and micropowder silica gel are mixed, sieved and mixed evenly, and then the content of this intermediate is determined, and the amount according to the specification is directly compressed into tablets...
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