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=ANDA203512"
符合检索条件的记录共 64 条，共 4 页，当前第 3 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
71335-0401-6 71335-0401 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA203512 Bryant Ranch Prepack SPIRONOLACTONE 50 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71335-0401-6)
71335-0304-2 71335-0304 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA203512 Bryant Ranch Prepack SPIRONOLACTONE 100 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (71335-0304-2)
71335-0304-3 71335-0304 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA203512 Bryant Ranch Prepack SPIRONOLACTONE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0304-3)
71335-0304-4 71335-0304 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA203512 Bryant Ranch Prepack SPIRONOLACTONE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0304-4)
16729-225-01 16729-225 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20170602 N/A ANDA ANDA203512 Accord Healthcare, Inc. SPIRONOLACTONE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16729-225-01)
16729-226-16 16729-226 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20170602 N/A ANDA ANDA203512 Accord Healthcare, Inc. SPIRONOLACTONE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (16729-226-16)
16729-227-01 16729-227 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20170602 N/A ANDA ANDA203512 Accord Healthcare, Inc. SPIRONOLACTONE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16729-227-01)
16729-227-16 16729-227 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20170602 N/A ANDA ANDA203512 Accord Healthcare, Inc. SPIRONOLACTONE 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (16729-227-16)
68071-4374-3 68071-4374 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20180405 N/A ANDA ANDA203512 NuCare Pharmaceuticals,Inc. SPIRONOLACTONE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-4374-3)
43063-832-01 43063-832 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20180131 N/A ANDA ANDA203512 PD-Rx Pharmaceuticals, Inc. SPIRONOLACTONE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-832-01)
43063-832-30 43063-832 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20180131 N/A ANDA ANDA203512 PD-Rx Pharmaceuticals, Inc. SPIRONOLACTONE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-832-30)
43063-832-60 43063-832 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20180612 N/A ANDA ANDA203512 PD-Rx Pharmaceuticals, Inc. SPIRONOLACTONE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-832-60)
43063-832-90 43063-832 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20180131 N/A ANDA ANDA203512 PD-Rx Pharmaceuticals, Inc. SPIRONOLACTONE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-832-90)
43063-835-30 43063-835 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20180213 N/A ANDA ANDA203512 PD-Rx Pharmaceuticals, Inc. SPIRONOLACTONE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-835-30)
43063-835-90 43063-835 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20180307 N/A ANDA ANDA203512 PD-Rx Pharmaceuticals, Inc. SPIRONOLACTONE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-835-90)
76420-062-01 76420-062 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20231003 N/A ANDA ANDA203512 Asclemed USA, Inc. SPIRONOLACTONE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-062-01)
76420-062-30 76420-062 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20200211 N/A ANDA ANDA203512 Asclemed USA, Inc. SPIRONOLACTONE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-062-30)
76420-062-60 76420-062 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20231003 N/A ANDA ANDA203512 Asclemed USA, Inc. SPIRONOLACTONE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-062-60)
76420-062-90 76420-062 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20231003 N/A ANDA ANDA203512 Asclemed USA, Inc. SPIRONOLACTONE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-062-90)
76420-063-30 76420-063 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20200211 N/A ANDA ANDA203512 Asclemed USA, Inc. SPIRONOLACTONE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-063-30)
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