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=ANDA213248"
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
62332-497-91 62332-497 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Inc. LURASIDONE HYDROCHLORIDE 80 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (62332-497-91)
62332-498-91 62332-498 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Inc. LURASIDONE HYDROCHLORIDE 120 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (62332-498-91)
62332-498-10 62332-498 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Inc. LURASIDONE HYDROCHLORIDE 120 mg/1 100 BLISTER PACK in 1 CARTON (62332-498-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
62332-498-30 62332-498 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Inc. LURASIDONE HYDROCHLORIDE 120 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (62332-498-30)
62332-498-71 62332-498 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Inc. LURASIDONE HYDROCHLORIDE 120 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (62332-498-71)
62332-498-90 62332-498 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Inc. LURASIDONE HYDROCHLORIDE 120 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (62332-498-90)
46708-494-10 46708-494 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Limited LURASIDONE HYDROCHLORIDE 20 mg/1 100 BLISTER PACK in 1 CARTON (46708-494-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
46708-494-30 46708-494 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Limited LURASIDONE HYDROCHLORIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (46708-494-30)
46708-494-71 46708-494 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Limited LURASIDONE HYDROCHLORIDE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (46708-494-71)
46708-494-90 46708-494 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Limited LURASIDONE HYDROCHLORIDE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (46708-494-90)
46708-494-91 46708-494 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Limited LURASIDONE HYDROCHLORIDE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (46708-494-91)
46708-495-10 46708-495 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Limited LURASIDONE HYDROCHLORIDE 40 mg/1 100 BLISTER PACK in 1 CARTON (46708-495-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
46708-495-30 46708-495 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Limited LURASIDONE HYDROCHLORIDE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (46708-495-30)
46708-495-71 46708-495 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Limited LURASIDONE HYDROCHLORIDE 40 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (46708-495-71)
46708-495-90 46708-495 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Limited LURASIDONE HYDROCHLORIDE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (46708-495-90)
46708-495-91 46708-495 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Limited LURASIDONE HYDROCHLORIDE 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (46708-495-91)
46708-496-10 46708-496 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Limited LURASIDONE HYDROCHLORIDE 60 mg/1 100 BLISTER PACK in 1 CARTON (46708-496-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
46708-496-30 46708-496 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Limited LURASIDONE HYDROCHLORIDE 60 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (46708-496-30)
46708-496-71 46708-496 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Limited LURASIDONE HYDROCHLORIDE 60 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (46708-496-71)
46708-496-90 46708-496 HUMAN PRESCRIPTION DRUG Lurasidone Hydrochloride Lurasidone Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA213248 Alembic Pharmaceuticals Limited LURASIDONE HYDROCHLORIDE 60 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (46708-496-90)
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