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=ANDA201003"
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
53002-2520-3 53002-2520 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20240101 N/A ANDA ANDA201003 RPK Pharmaceuticals, Inc. RISPERIDONE 1 mg/1 30 TABLET in 1 BOTTLE (53002-2520-3)
68071-2706-6 68071-2706 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20220519 N/A ANDA ANDA201003 NuCare Pharmaceuticals,Inc. RISPERIDONE 2 mg/1 60 TABLET in 1 BOTTLE (68071-2706-6)
70518-0364-0 70518-0364 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20170327 N/A ANDA ANDA201003 REMEDYREPACK INC. RISPERIDONE 1 mg/1 30 TABLET in 1 BLISTER PACK (70518-0364-0)
70518-0364-1 70518-0364 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20210430 N/A ANDA ANDA201003 REMEDYREPACK INC. RISPERIDONE 1 mg/1 30 TABLET in 1 BLISTER PACK (70518-0364-1)
27241-001-06 27241-001 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20140328 N/A ANDA ANDA201003 Ajanta Pharma USA Inc. RISPERIDONE 1 mg/1 60 TABLET in 1 BOTTLE (27241-001-06)
27241-001-50 27241-001 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20140328 N/A ANDA ANDA201003 Ajanta Pharma USA Inc. RISPERIDONE 1 mg/1 500 TABLET in 1 BOTTLE (27241-001-50)
27241-002-06 27241-002 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20140328 N/A ANDA ANDA201003 Ajanta Pharma USA Inc. RISPERIDONE .25 mg/1 60 TABLET in 1 BOTTLE (27241-002-06)
27241-002-50 27241-002 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20140328 N/A ANDA ANDA201003 Ajanta Pharma USA Inc. RISPERIDONE .25 mg/1 500 TABLET in 1 BOTTLE (27241-002-50)
27241-003-06 27241-003 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20140328 N/A ANDA ANDA201003 Ajanta Pharma USA Inc. RISPERIDONE .5 mg/1 60 TABLET in 1 BOTTLE (27241-003-06)
27241-003-50 27241-003 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20140328 N/A ANDA ANDA201003 Ajanta Pharma USA Inc. RISPERIDONE .5 mg/1 500 TABLET in 1 BOTTLE (27241-003-50)
27241-004-06 27241-004 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20140328 N/A ANDA ANDA201003 Ajanta Pharma USA Inc. RISPERIDONE 2 mg/1 60 TABLET in 1 BOTTLE (27241-004-06)
27241-004-50 27241-004 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20140328 N/A ANDA ANDA201003 Ajanta Pharma USA Inc. RISPERIDONE 2 mg/1 500 TABLET in 1 BOTTLE (27241-004-50)
27241-005-06 27241-005 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20140328 N/A ANDA ANDA201003 Ajanta Pharma USA Inc. RISPERIDONE 3 mg/1 60 TABLET in 1 BOTTLE (27241-005-06)
27241-005-50 27241-005 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20140328 N/A ANDA ANDA201003 Ajanta Pharma USA Inc. RISPERIDONE 3 mg/1 500 TABLET in 1 BOTTLE (27241-005-50)
27241-006-06 27241-006 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20140328 N/A ANDA ANDA201003 Ajanta Pharma USA Inc. RISPERIDONE 4 mg/1 60 TABLET in 1 BOTTLE (27241-006-06)
27241-006-50 27241-006 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20140328 N/A ANDA ANDA201003 Ajanta Pharma USA Inc. RISPERIDONE 4 mg/1 500 TABLET in 1 BOTTLE (27241-006-50)
43063-908-07 43063-908 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20220811 N/A ANDA ANDA201003 PD-Rx Pharmaceuticals, Inc. RISPERIDONE 1 mg/1 7 TABLET in 1 BOTTLE, PLASTIC (43063-908-07)
43063-908-30 43063-908 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20181127 N/A ANDA ANDA201003 PD-Rx Pharmaceuticals, Inc. RISPERIDONE 1 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (43063-908-30)
43063-908-60 43063-908 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20181127 N/A ANDA ANDA201003 PD-Rx Pharmaceuticals, Inc. RISPERIDONE 1 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (43063-908-60)
70518-1502-0 70518-1502 HUMAN PRESCRIPTION DRUG RISPERIDONE RISPERIDONE TABLET ORAL 20181008 N/A ANDA ANDA201003 REMEDYREPACK INC. RISPERIDONE 3 mg/1 30 TABLET in 1 BLISTER PACK (70518-1502-0)
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