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=ANDA205936"
符合检索条件的记录共 44 条，共 3 页，当前第 2 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
70518-4512-0 70518-4512 HUMAN PRESCRIPTION DRUG spironolactone spironolactone TABLET, FILM COATED ORAL 20251028 N/A ANDA ANDA205936 REMEDYREPACK INC. SPIRONOLACTONE 100 mg/1 100 POUCH in 1 BOX (70518-4512-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4512-1)
60687-476-01 60687-476 HUMAN PRESCRIPTION DRUG Spironolactone Spironolactone TABLET ORAL 20190606 N/A ANDA ANDA205936 American Health Packaging SPIRONOLACTONE 50 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-476-01) / 1 TABLET in 1 BLISTER PACK (60687-476-11)
60687-487-01 60687-487 HUMAN PRESCRIPTION DRUG Spironolactone Spironolactone TABLET ORAL 20190606 N/A ANDA ANDA205936 American Health Packaging SPIRONOLACTONE 100 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-487-01) / 1 TABLET in 1 BLISTER PACK (60687-487-11)
70771-1027-3 70771-1027 HUMAN PRESCRIPTION DRUG spironolactone spironolactone TABLET, FILM COATED ORAL 20180815 N/A ANDA ANDA205936 Zydus Lifesciences Limited SPIRONOLACTONE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70771-1027-3)
70771-1027-1 70771-1027 HUMAN PRESCRIPTION DRUG spironolactone spironolactone TABLET, FILM COATED ORAL 20180815 N/A ANDA ANDA205936 Zydus Lifesciences Limited SPIRONOLACTONE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1027-1)
70771-1027-0 70771-1027 HUMAN PRESCRIPTION DRUG spironolactone spironolactone TABLET, FILM COATED ORAL 20180815 N/A ANDA ANDA205936 Zydus Lifesciences Limited SPIRONOLACTONE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1027-0)
68382-660-01 68382-660 HUMAN PRESCRIPTION DRUG spironolactone spironolactone TABLET, FILM COATED ORAL 20180815 N/A ANDA ANDA205936 Zydus Pharmaceuticals (USA) Inc. SPIRONOLACTONE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-660-01)
68382-660-16 68382-660 HUMAN PRESCRIPTION DRUG spironolactone spironolactone TABLET, FILM COATED ORAL 20180815 N/A ANDA ANDA205936 Zydus Pharmaceuticals (USA) Inc. SPIRONOLACTONE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68382-660-16)
68382-660-30 68382-660 HUMAN PRESCRIPTION DRUG spironolactone spironolactone TABLET, FILM COATED ORAL 20180815 N/A ANDA ANDA205936 Zydus Pharmaceuticals (USA) Inc. SPIRONOLACTONE 25 mg/1 10 BLISTER PACK in 1 CARTON (68382-660-30) / 10 TABLET, FILM COATED in 1 BLISTER PACK
68382-661-01 68382-661 HUMAN PRESCRIPTION DRUG spironolactone spironolactone TABLET, FILM COATED ORAL 20180815 N/A ANDA ANDA205936 Zydus Pharmaceuticals (USA) Inc. SPIRONOLACTONE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-661-01)
68382-661-05 68382-661 HUMAN PRESCRIPTION DRUG spironolactone spironolactone TABLET, FILM COATED ORAL 20180815 N/A ANDA ANDA205936 Zydus Pharmaceuticals (USA) Inc. SPIRONOLACTONE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68382-661-05)
68382-661-06 68382-661 HUMAN PRESCRIPTION DRUG spironolactone spironolactone TABLET, FILM COATED ORAL 20180815 N/A ANDA ANDA205936 Zydus Pharmaceuticals (USA) Inc. SPIRONOLACTONE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68382-661-06)
68382-661-10 68382-661 HUMAN PRESCRIPTION DRUG spironolactone spironolactone TABLET, FILM COATED ORAL 20180815 N/A ANDA ANDA205936 Zydus Pharmaceuticals (USA) Inc. SPIRONOLACTONE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (68382-661-10)
68382-661-16 68382-661 HUMAN PRESCRIPTION DRUG spironolactone spironolactone TABLET, FILM COATED ORAL 20180815 N/A ANDA ANDA205936 Zydus Pharmaceuticals (USA) Inc. SPIRONOLACTONE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68382-661-16)
68382-661-30 68382-661 HUMAN PRESCRIPTION DRUG spironolactone spironolactone TABLET, FILM COATED ORAL 20180815 N/A ANDA ANDA205936 Zydus Pharmaceuticals (USA) Inc. SPIRONOLACTONE 50 mg/1 10 BLISTER PACK in 1 CARTON (68382-661-30) / 10 TABLET, FILM COATED in 1 BLISTER PACK
68382-662-01 68382-662 HUMAN PRESCRIPTION DRUG spironolactone spironolactone TABLET, FILM COATED ORAL 20180815 N/A ANDA ANDA205936 Zydus Pharmaceuticals (USA) Inc. SPIRONOLACTONE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-662-01)
68382-662-05 68382-662 HUMAN PRESCRIPTION DRUG spironolactone spironolactone TABLET, FILM COATED ORAL 20180815 N/A ANDA ANDA205936 Zydus Pharmaceuticals (USA) Inc. SPIRONOLACTONE 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68382-662-05)
68382-662-06 68382-662 HUMAN PRESCRIPTION DRUG spironolactone spironolactone TABLET, FILM COATED ORAL 20180815 N/A ANDA ANDA205936 Zydus Pharmaceuticals (USA) Inc. SPIRONOLACTONE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68382-662-06)
68382-662-10 68382-662 HUMAN PRESCRIPTION DRUG spironolactone spironolactone TABLET, FILM COATED ORAL 20180815 N/A ANDA ANDA205936 Zydus Pharmaceuticals (USA) Inc. SPIRONOLACTONE 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (68382-662-10)
68382-662-16 68382-662 HUMAN PRESCRIPTION DRUG spironolactone spironolactone TABLET, FILM COATED ORAL 20180815 N/A ANDA ANDA205936 Zydus Pharmaceuticals (USA) Inc. SPIRONOLACTONE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68382-662-16)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase