Medicine composition for treating upper respiratory tract infection and its prepn process
A technology of upper respiratory tract and composition, which is applied in the field of pharmaceutical composition for treating upper respiratory tract infection and its preparation, which can solve the problems of inconvenient use of injections, inconvenient carrying of oral liquids, and prone to allergic reactions, etc. , Low production cost, good dispersion effect
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Embodiment 1
[0031] Prescription: Honeysuckle extract 10g, Scutellaria baicalensis extract 4g, crospovidone 6g, silicon dioxide 0.5g, microcrystalline cellulose 2.2g, talcum powder 0.7g, sodium carboxymethyl starch 2g, magnesium stearate 0.32g , stevia 0.3g;
[0032] Preparation method: mix the powder of honeysuckle extract and baicalin extract with microcrystalline cellulose, sodium carboxymethyl starch, and crospovidone, then add silicon dioxide, magnesium stearate, etc., mix and directly compress into tablets. Promptly get the drug dispersible tablet of the present invention.
[0033] The obtained dispersible tablets have the following characteristics:
[0034] Uniformity of dispersion: in accordance with the provisions of the Pharmacopoeia, in water at 20°C ± 1°C, it should be completely disintegrated within three minutes and pass through the No. 2 sieve.
[0035] powder direct compression
Embodiment 2
[0037] Prescription: Honeysuckle extract 8g, Scutellaria baicalensis extract 8g, crospovidone 4g, silicon dioxide 0.3g, microcrystalline cellulose 1.5g, talcum powder 0.3g, sodium carboxymethyl starch 3g, magnesium stearate 0.1g , stevia 0.15g;
[0038] Preparation method: mix the powder of honeysuckle extract and baicalin extract with microcrystalline cellulose, sodium carboxymethyl starch, and crospovidone, then add silicon dioxide, magnesium stearate, etc., mix and directly compress into tablets. Promptly get the drug dispersible tablet of the present invention.
[0039] The obtained dispersible tablets have the following characteristics:
[0040] Uniformity of dispersion: in accordance with the provisions of the Pharmacopoeia, in water at 20°C ± 1°C, it should be completely disintegrated within three minutes and pass through the No. 2 sieve.
[0041] powder direct compression
Embodiment 3
[0043] Prescription: Honeysuckle extract 7g, Scutellaria baicalensis extract 2.5g, crospovidone 8g, silicon dioxide 0.7g, microcrystalline cellulose 4g, talcum powder 0.8g, sodium carboxymethyl starch 3g, magnesium stearate 0.42g , stevia 0.5g;
[0044] Preparation method: mix the powder of honeysuckle extract and baicalin extract with microcrystalline cellulose, sodium carboxymethyl starch, and crospovidone, then add silicon dioxide, magnesium stearate, etc., mix and directly compress into tablets. Promptly get the drug dispersible tablet of the present invention.
[0045] The obtained dispersible tablets have the following characteristics:
[0046] Uniformity of dispersion: in accordance with the provisions of the Pharmacopoeia, in water at 20°C ± 1°C, it should be completely disintegrated within three minutes and pass through the No. 2 sieve.
[0047] powder direct compression
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