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"
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
71610-970-60 71610-970 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 20251203 N/A ANDA ANDA089424 Aphena Pharma Solutions - Tennessee, LLC SPIRONOLACTONE 25 mg/1 90 TABLET in 1 BOTTLE (71610-970-60)
71610-970-80 71610-970 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 20251203 N/A ANDA ANDA089424 Aphena Pharma Solutions - Tennessee, LLC SPIRONOLACTONE 25 mg/1 180 TABLET in 1 BOTTLE (71610-970-80)
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)
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)
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)
71610-742-30 71610-742 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 20231026 N/A ANDA ANDA089424 Aphena Pharma Solutions - Tennessee, LLC SPIRONOLACTONE 25 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (71610-742-30)
71610-742-45 71610-742 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 20231010 N/A ANDA ANDA089424 Aphena Pharma Solutions - Tennessee, LLC SPIRONOLACTONE 25 mg/1 45 TABLET in 1 BOTTLE, PLASTIC (71610-742-45)
71610-742-60 71610-742 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 20231010 N/A ANDA ANDA089424 Aphena Pharma Solutions - Tennessee, LLC SPIRONOLACTONE 25 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (71610-742-60)
71610-742-80 71610-742 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 20231010 N/A ANDA ANDA089424 Aphena Pharma Solutions - Tennessee, LLC SPIRONOLACTONE 25 mg/1 180 TABLET in 1 BOTTLE, PLASTIC (71610-742-80)
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)
71335-2366-6 71335-2366 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 20240430 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 25 mg/1 7 TABLET in 1 BOTTLE, PLASTIC (71335-2366-6)
71335-2366-7 71335-2366 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 20240430 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 25 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (71335-2366-7)
71335-2366-8 71335-2366 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 20240430 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 25 mg/1 180 TABLET in 1 BOTTLE, PLASTIC (71335-2366-8)
71335-2366-9 71335-2366 HUMAN PRESCRIPTION DRUG SPIRONOLACTONE SPIRONOLACTONE TABLET ORAL 20240430 N/A ANDA ANDA089424 Bryant Ranch Prepack SPIRONOLACTONE 25 mg/1 45 TABLET in 1 BOTTLE, PLASTIC (71335-2366-9)
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)
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