Gabapentin tablet and preparation method thereof
A technology for gabapentin tablets and gabapentin is applied in the directions of pill delivery, pharmaceutical formulations, medical preparations of inactive ingredients, etc., can solve the problems of low drug content, undisclosed inclusion of gabapentin, and no research, and achieves content uniformity that meets the requirements of Effect
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Embodiment 1
[0029] Gabapentin tablets are prepared from the following medicinal components:
[0030]
[0031] Preparation
[0032] Gabapentin and lactose are micronized at a ratio of 1:20 for use; prepare a 15% concentration of PVP K30 aqueous solution for use; weigh the prescribed amount of gabapentin, lactose, and starch and mix them evenly, add PVP K30 aqueous solution for granulation, dry, and add the corresponding The prescription amount of magnesium stearate is mixed evenly, the content of the mixture is measured, the tablet weight is calculated, and the tablet is pressed to obtain it.
[0033] The prepared gabapentin tablets have the following characteristics:
[0034] Content uniformity inspection: qualified. Disintegration time limit inspection: complete disintegration within 5 minutes, the disintegration phenomenon is the same as the original development.
Embodiment 2
[0036] Gabapentin tablets are prepared from the following medicinal components:
[0037]
[0038] Preparation
[0039] Gabapentin and lactose are micronized at a ratio of 1:20 for use; prepare a 15% concentration of PVP K30 aqueous solution for use; weigh the prescribed amount of gabapentin, lactose, and starch and mix them evenly, add PVP K30 aqueous solution for granulation, dry, and add the corresponding The prescription amount of magnesium stearate is mixed evenly, the content of the mixture is measured, the tablet weight is calculated, and the tablet is pressed to obtain it.
[0040] The prepared gabapentin tablets have the following characteristics: content uniformity inspection: qualified. Disintegration time limit inspection: complete disintegration within 5 minutes.
Embodiment 3
[0042] Gabapentin tablets are prepared from the following medicinal components:
[0043]
[0044]
[0045] Preparation
[0046] Gabapentin and lactose are micronized at a ratio of 1:20 for use; prepare a 15% concentration of PVP K30 aqueous solution for use; weigh the prescribed amount of gabapentin, lactose, and starch and mix them evenly, add PVP K30 aqueous solution for granulation, dry, and add the corresponding The prescription amount of magnesium stearate is mixed evenly, the content of the mixture is measured, the tablet weight is calculated, and the tablet is pressed to obtain it.
[0047] The prepared gabapentin tablets have the following characteristics: content uniformity inspection: qualified. Disintegration time limit inspection: complete disintegration within 5 minutes.
[0048] The specific values of the dissolution profile of each embodiment of the present invention and the reference preparation (commercially available ordinary tablets, Hainan Serike Pharmaceutical,...
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