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"
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
71335-0304-1 71335-0304 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA203512 Bryant Ranch Prepack SPIRONOLACTONE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-0304-1)
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)
71335-0304-5 71335-0304 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20220209 N/A ANDA ANDA203512 Bryant Ranch Prepack SPIRONOLACTONE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-0304-5)
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)
71205-148-30 71205-148 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA203512 Proficient Rx LP SPIRONOLACTONE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-148-30)
71205-148-60 71205-148 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA203512 Proficient Rx LP SPIRONOLACTONE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-148-60)
71205-148-90 71205-148 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA203512 Proficient Rx LP SPIRONOLACTONE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-148-90)
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)
71205-146-30 71205-146 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA203512 Proficient Rx LP SPIRONOLACTONE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-146-30)
71205-146-60 71205-146 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA203512 Proficient Rx LP SPIRONOLACTONE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-146-60)
71205-146-90 71205-146 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA203512 Proficient Rx LP SPIRONOLACTONE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-146-90)
68071-3375-1 68071-3375 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20170711 N/A ANDA ANDA203512 NuCare Pharmaceuticals, Inc. SPIRONOLACTONE 25 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (68071-3375-1)
68071-3375-3 68071-3375 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20170711 N/A ANDA ANDA203512 NuCare Pharmaceuticals, Inc. SPIRONOLACTONE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3375-3)
68071-3375-6 68071-3375 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20170711 N/A ANDA ANDA203512 NuCare Pharmaceuticals, Inc. SPIRONOLACTONE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-3375-6)
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