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=ANDA089424"
符合检索条件的记录共 121 条，共 7 页，当前第 3 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
71335-2207-1 71335-2207 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20230804 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2207-1)
63629-1062-1 63629-1062 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 19860723 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 25 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (63629-1062-1)
53489-329-03 53489-329 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 19860723 N/A ANDA ANDA089424 Sun Pharmaceutical Industries, Inc. SPIRONOLACTONE 100 mg/1 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-03)
53489-329-05 53489-329 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 19860723 N/A ANDA ANDA089424 Sun Pharmaceutical Industries, Inc. SPIRONOLACTONE 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-05)
53489-329-10 53489-329 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 19860723 N/A ANDA ANDA089424 Sun Pharmaceutical Industries, Inc. SPIRONOLACTONE 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-10)
71205-830-30 71205-830 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20230818 N/A ANDA ANDA089424 Proficient Rx LP SPIRONOLACTONE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-830-30)
71205-830-60 71205-830 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20230818 N/A ANDA ANDA089424 Proficient Rx LP SPIRONOLACTONE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-830-60)
71205-830-90 71205-830 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20230818 N/A ANDA ANDA089424 Proficient Rx LP SPIRONOLACTONE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-830-90)
76420-557-01 76420-557 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20230407 N/A ANDA ANDA089424 Asclemed USA, Inc. SPIRONOLACTONE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-557-01)
76420-557-30 76420-557 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20230407 N/A ANDA ANDA089424 Asclemed USA, Inc. SPIRONOLACTONE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-557-30)
76420-557-60 76420-557 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20230407 N/A ANDA ANDA089424 Asclemed USA, Inc. SPIRONOLACTONE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-557-60)
76420-557-90 76420-557 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20230407 N/A ANDA ANDA089424 Asclemed USA, Inc. SPIRONOLACTONE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-557-90)
63629-1067-1 63629-1067 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20200921 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-1067-1)
76420-558-01 76420-558 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20230407 N/A ANDA ANDA089424 Asclemed USA, Inc. SPIRONOLACTONE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-558-01)
76420-558-30 76420-558 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20230407 N/A ANDA ANDA089424 Asclemed USA, Inc. SPIRONOLACTONE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-558-30)
76420-558-60 76420-558 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20230407 N/A ANDA ANDA089424 Asclemed USA, Inc. SPIRONOLACTONE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-558-60)
76420-558-90 76420-558 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20230407 N/A ANDA ANDA089424 Asclemed USA, Inc. SPIRONOLACTONE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-558-90)
50090-6432-0 50090-6432 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20230411 N/A ANDA ANDA089424 A-S Medication Solutions SPIRONOLACTONE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6432-0)
50090-6432-1 50090-6432 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20230411 N/A ANDA ANDA089424 A-S Medication Solutions SPIRONOLACTONE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-6432-1)
71335-2846-1 71335-2846 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 20251028 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 25 mg/1 100 TABLET in 1 BOTTLE (71335-2846-1)
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