美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA208047"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
13668-509-30 13668-509 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, FILM COATED ORAL 20230217 N/A ANDA ANDA208047 Torrent Pharmaceuticals Limited LURASIDONE HYDROCHLORIDE 60 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (13668-509-30)
43598-351-78 43598-351 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA208047 Dr. Reddys Laboratories Inc LURASIDONE HYDROCHLORIDE 20 mg/1 10 BLISTER PACK in 1 CARTON (43598-351-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-351-79)
43598-352-05 43598-352 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA208047 Dr. Reddys Laboratories Inc LURASIDONE HYDROCHLORIDE 40 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (43598-352-05)
43598-352-30 43598-352 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA208047 Dr. Reddys Laboratories Inc LURASIDONE HYDROCHLORIDE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (43598-352-30)
43598-352-78 43598-352 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA208047 Dr. Reddys Laboratories Inc LURASIDONE HYDROCHLORIDE 40 mg/1 10 BLISTER PACK in 1 CARTON (43598-352-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-352-79)
43598-352-90 43598-352 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA208047 Dr. Reddys Laboratories Inc LURASIDONE HYDROCHLORIDE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (43598-352-90)
43598-353-05 43598-353 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA208047 Dr. Reddys Laboratories Inc LURASIDONE HYDROCHLORIDE 60 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (43598-353-05)
43598-353-30 43598-353 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA208047 Dr. Reddys Laboratories Inc LURASIDONE HYDROCHLORIDE 60 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (43598-353-30)
43598-353-78 43598-353 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA208047 Dr. Reddys Laboratories Inc LURASIDONE HYDROCHLORIDE 60 mg/1 10 BLISTER PACK in 1 CARTON (43598-353-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-353-79)
43598-353-90 43598-353 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA208047 Dr. Reddys Laboratories Inc LURASIDONE HYDROCHLORIDE 60 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (43598-353-90)
43598-354-05 43598-354 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA208047 Dr. Reddys Laboratories Inc LURASIDONE HYDROCHLORIDE 80 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (43598-354-05)
43598-354-30 43598-354 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA208047 Dr. Reddys Laboratories Inc LURASIDONE HYDROCHLORIDE 80 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (43598-354-30)
43598-354-78 43598-354 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA208047 Dr. Reddys Laboratories Inc LURASIDONE HYDROCHLORIDE 80 mg/1 10 BLISTER PACK in 1 CARTON (43598-354-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-354-79)
43598-354-90 43598-354 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA208047 Dr. Reddys Laboratories Inc LURASIDONE HYDROCHLORIDE 80 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (43598-354-90)
43598-351-30 43598-351 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA208047 Dr. Reddys Laboratories Inc LURASIDONE HYDROCHLORIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (43598-351-30)
43598-351-05 43598-351 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA208047 Dr. Reddys Laboratories Inc LURASIDONE HYDROCHLORIDE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (43598-351-05)
43598-351-90 43598-351 HUMAN PRESCRIPTION DRUG Lurasidone hydrochloride Lurasidone hydrochloride TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA208047 Dr. Reddys Laboratories Inc LURASIDONE HYDROCHLORIDE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (43598-351-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase