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 5 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
53489-328-07 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)
63629-5341-1 63629-5341 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20140516 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63629-5341-1)
63629-5341-2 63629-5341 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20171016 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63629-5341-2)
63629-5341-3 63629-5341 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20160218 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63629-5341-3)
63629-5341-4 63629-5341 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20230309 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (63629-5341-4)
63629-5341-5 63629-5341 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20230309 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 50 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (63629-5341-5)
63629-5341-6 63629-5341 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET, FILM COATED ORAL 20230309 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 50 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (63629-5341-6)
70518-4350-0 70518-4350 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 20250530 N/A ANDA ANDA089424 REMEDYREPACK INC. SPIRONOLACTONE 25 mg/1 100 POUCH in 1 BOX (70518-4350-0) / 1 TABLET in 1 POUCH (70518-4350-1)
63629-8539-1 63629-8539 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 19960723 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 25 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (63629-8539-1)
71335-2205-1 71335-2205 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 20230804 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 25 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (71335-2205-1)
71335-2217-1 71335-2217 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 20230919 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 25 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (71335-2217-1)
71335-2301-1 71335-2301 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 20231201 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 25 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (71335-2301-1)
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