Details for Patent: 9,017,722
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Title: | Pharmaceutical composition containing as an active ingredient 5-methyl-1-phenyl-2-(1H)-pyridone |
Abstract: | A tablet characterized by comprising 5-methyl-1-phenyl-2-(1H)-pyridone as the main ingredient and, based on the main ingredient, 10 to 50 wt. % excipient, 5 to 40 wt. % disintegrator, 1 to 10 wt. % binder, 0.5 to 5 wt. % lubricant, 2 to 6 wt. % coating basis, and 0.05 to 3 wt. % light-shielding agent, wherein the odor or bitterness of the 5-methyl-1-phenyl-2-(1H)-pyridone is masked and the light stability is improved. |
Inventor(s): | Kiyonaka; Gakuji (Amagasaki, JP), Furuya; Yoshihiro (Amagasaki, JP), Suzuki; Yusuke (Settsu, JP) |
Assignee: | Intermune, Inc. (Brisbane, CA) |
Filing Date: | Oct 26, 2012 |
Application Number: | 13/662,221 |
Claims: | 1. A tablet comprising an amount of 5-methyl-1-phenyl-2-(1H)-pyridone, and further comprising 10 to 50 wt % excipient selected from lactose, corn starch, crystalline cellulose, or any mixture thereof, 5 to 40 wt % disintegrant selected from carmellose calcium, carmellose sodium, croscarmellose sodium, low substituted hydroxypropylcellulose, cross-linked polyvinylpyrrolidone, or any mixture thereof, 1 to 10 wt % binder selected from hydroxypropylcellulose and polyvinylpyrrolidone, or any mixture thereof, and 0.5 to 5 wt. % lubricant selected from magnesium stearate, talc, or any mixture thereof, the wt. % being based on the weight of the 5-methyl-1-phenyl-2-(1H)-pyridone. 2. A tablet according to claim 1, wherein the tablet has a weight ranging from 100 to 1000 mg. 3. A tablet according to claim 1 or 2, wherein the table comprises 10 to 85% of the 5-methyl-1-phenyl-2-(1H)-pyridone by weight based on the total weight of the tablet. 4. A tablet according to claim 1, wherein the amount of the 5-methyl-1-phenyl-2-(1H)-pyridone ranges from 200 mg to 400 mg. 5. A tablet according to claim 1, further comprising a light-shielding agent. 6. A tablet according to claim 5, wherein the light-shielding agent is present in an amount ranging from 0.05 to 3 wt. %. 7. A tablet according to claim 1, further comprising 2 to 6 wt. % coating basis, and 0.05 to 3 wt. % light-shielding agent. 8. A tablet according to claim 7, further comprising 0.01 to 1 wt. % plasticizer. 9. A tablet according to claim 1, further comprising a coating layer comprising 2 to 6 wt. % coating basis and 0.05 to 3 wt. % light-shielding agent. 10. A tablet as claimed in claim 9, wherein the coating layer further comprises 0.01 to 1 wt. % plasticizer. 11. A tablet comprising: a core comprising an amount of 5-methyl-1-phenyl-2-(1H)-pyridone, 10 to 50 wt. % excipient selected from lactose, corn starch, crystalline cellulose, or any mixture thereof; 5 to 40 wt. % disintegrator selected from carmellose calcium, carmellose sodium, croscarmellose sodium, low substituted hydroxypropylcellulose, cross-linked polyvinylpyrrolidone, or any mixture thereof; 1 to 10 wt. % binder selected from hydroxypropylcellulose and polyvinylpyrrolidone, or any mixture thereof; and 0.5 to 5 wt. % lubricant selected from magnesium stearate, talc, or any mixture thereof, and a coating layer comprising 2 to 6 wt. % coating basis selected from hydroxypropylmethylcellulose, hydroxypropylcellulose, or any mixture thereof; 0.01 to 1 wt. % plasticizer selected from triethyl citrate, triacetin, or any mixture thereof; and 0.05 to 3 wt. % light-shielding agent selected from titanium oxide, ferric oxide, or any mixture thereof, wherein the wt % are based on the weight of the 5-methyl-1-phenyl-2-(1H)-pyridone. 12. A tablet according to claim 11, wherein the core comprises 10 to 50 wt. % lactose, 5 to 40 wt. % carmellose calcium, 1 to 10 wt. % hydroxypropylcellulose, and 0.5 to 5 wt. magnesium, and the coating layer comprises 2 to 6 wt. % hydroxypropylmethylcellulose, 0.01 to 1 wt. % triethyl citrate, and 0.05 to 3 wt. % titanium oxide. 13. A tablet comprising: a core comprising an amount of 5-methyl-1-phenyl-2-(1H)-pyridone, 20 to 30 wt. % excipient selected from lactose, corn starch, crystalline cellulose, or any mixture thereof; 7.5 to 15 wt. % disintegrator selected from carmellose calcium, carmellose sodium, croscarmellose sodium, low substituted hydroxypropylcellulose, cross-linked polyvinylpyrrolidone, or any mixture thereof; 2 to 5 wt. % binder selected from hydroxypropylcellulose, polyvinylpyrrolidone, or any mixture thereof; and 0.5 to 3 wt. % lubricant selected from magnesium stearate, talc, or any mixture thereof, and a coating layer comprising 2 to 4 wt. % coating basis selected from hydroxypropylmethylcellulose, hydroxypropylcellulose, or any mixture thereof; 0.01 to 1 wt. % plasticizer selected from triethyl citrate, triacetin, or any mixture thereof; and 0.8 to 3 wt. % titanium oxide as a light-shielding agent, wherein the wt % are based on the weight of the 5-methyl-1-phenyl-2-(1H)-pyridone. 14. A tablet according to claim 13, wherein the core comprises 20 to 30 wt. % lactose, 7.5 to 15 wt. % carmellose calcium, 2 to 5 wt. % hydroxypropylcellulose, and 0.5 to 3 wt. magnesium stearate, and the coating layer comprises 2 to 4 wt. % hydroxypropylmethylcellulose, 0.01 to 1 wt. % triethyl citrate and 0.8 to 3 wt. % titanium oxide. |