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 125 条，共 7 页，当前第 6 页 ，可点击列名称排序
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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
53489-143-01 53489-143 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 19860723 N/A ANDA ANDA089424 Sun Pharmaceutical Industries, Inc. SPIRONOLACTONE 25 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (53489-143-01)
53489-143-05 53489-143 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 19860723 N/A ANDA ANDA089424 Sun Pharmaceutical Industries, Inc. SPIRONOLACTONE 25 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (53489-143-05)
53489-143-10 53489-143 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 19960723 N/A ANDA ANDA089424 Sun Pharmaceutical Industries, Inc. SPIRONOLACTONE 25 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (53489-143-10)
53489-328-01 53489-328 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 19860723 N/A ANDA ANDA089424 Sun Pharmaceutical Industries, Inc. SPIRONOLACTONE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-01)
53489-328-02 53489-328 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 19860723 N/A ANDA ANDA089424 Sun Pharmaceutical Industries, Inc. SPIRONOLACTONE 50 mg/1 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-02)
53489-328-03 53489-328 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 19860723 N/A ANDA ANDA089424 Sun Pharmaceutical Industries, Inc. SPIRONOLACTONE 50 mg/1 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-03)
53489-328-05 53489-328 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 19860723 N/A ANDA ANDA089424 Sun Pharmaceutical Industries, Inc. SPIRONOLACTONE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-05)
53489-328-06 53489-328 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 19860723 N/A ANDA ANDA089424 Sun Pharmaceutical Industries, Inc. SPIRONOLACTONE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-06)
53489-328-07 53489-328 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 19860723 N/A ANDA ANDA089424 Sun Pharmaceutical Industries, Inc. SPIRONOLACTONE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-07)
53489-328-10 53489-328 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 19860723 N/A ANDA ANDA089424 Sun Pharmaceutical Industries, Inc. SPIRONOLACTONE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-10)
53489-329-01 53489-329 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 19860723 N/A ANDA ANDA089424 Sun Pharmaceutical Industries, Inc. SPIRONOLACTONE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-01)
53489-329-02 53489-329 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 19860723 N/A ANDA ANDA089424 Sun Pharmaceutical Industries, Inc. SPIRONOLACTONE 100 mg/1 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-02)
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)
53489-329-06 53489-329 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 19860723 N/A ANDA ANDA089424 Sun Pharmaceutical Industries, Inc. SPIRONOLACTONE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-06)
53489-329-07 53489-329 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 19860723 N/A ANDA ANDA089424 Sun Pharmaceutical Industries, Inc. SPIRONOLACTONE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-07)
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)
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)
71335-2887-1 71335-2887 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20251028 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-2887-1)
50090-6408-0 50090-6408 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20230323 N/A ANDA ANDA089424 A-S Medication Solutions SPIRONOLACTONE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (50090-6408-0)
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