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=ANDA203974"
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
71335-1838-0 71335-1838 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20241031 N/A ANDA ANDA203974 Bryant Ranch Prepack METRONIDAZOLE 250 mg/1 7 TABLET in 1 BOTTLE (71335-1838-0)
71335-1838-1 71335-1838 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20211123 N/A ANDA ANDA203974 Bryant Ranch Prepack METRONIDAZOLE 250 mg/1 21 TABLET in 1 BOTTLE (71335-1838-1)
71335-1838-2 71335-1838 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20210614 N/A ANDA ANDA203974 Bryant Ranch Prepack METRONIDAZOLE 250 mg/1 30 TABLET in 1 BOTTLE (71335-1838-2)
71335-1838-3 71335-1838 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20210514 N/A ANDA ANDA203974 Bryant Ranch Prepack METRONIDAZOLE 250 mg/1 20 TABLET in 1 BOTTLE (71335-1838-3)
71335-1838-4 71335-1838 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20241031 N/A ANDA ANDA203974 Bryant Ranch Prepack METRONIDAZOLE 250 mg/1 60 TABLET in 1 BOTTLE (71335-1838-4)
71335-1838-5 71335-1838 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20211101 N/A ANDA ANDA203974 Bryant Ranch Prepack METRONIDAZOLE 250 mg/1 28 TABLET in 1 BOTTLE (71335-1838-5)
71335-1838-6 71335-1838 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20231211 N/A ANDA ANDA203974 Bryant Ranch Prepack METRONIDAZOLE 250 mg/1 14 TABLET in 1 BOTTLE (71335-1838-6)
71335-1838-7 71335-1838 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20241031 N/A ANDA ANDA203974 Bryant Ranch Prepack METRONIDAZOLE 250 mg/1 40 TABLET in 1 BOTTLE (71335-1838-7)
71335-1838-8 71335-1838 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20241031 N/A ANDA ANDA203974 Bryant Ranch Prepack METRONIDAZOLE 250 mg/1 42 TABLET in 1 BOTTLE (71335-1838-8)
71335-1838-9 71335-1838 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20210430 N/A ANDA ANDA203974 Bryant Ranch Prepack METRONIDAZOLE 250 mg/1 56 TABLET in 1 BOTTLE (71335-1838-9)
70518-3110-5 70518-3110 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20240930 N/A ANDA ANDA203974 REMEDYREPACK INC. METRONIDAZOLE 500 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (70518-3110-5)
70518-3110-6 70518-3110 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20241125 N/A ANDA ANDA203974 REMEDYREPACK INC. METRONIDAZOLE 500 mg/1 4 TABLET in 1 BOTTLE, PLASTIC (70518-3110-6)
70518-3110-7 70518-3110 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20250108 N/A ANDA ANDA203974 REMEDYREPACK INC. METRONIDAZOLE 500 mg/1 30 TABLET in 1 BLISTER PACK (70518-3110-7)
71335-1922-0 71335-1922 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20241031 N/A ANDA ANDA203974 Bryant Ranch Prepack METRONIDAZOLE 500 mg/1 40 TABLET in 1 BOTTLE (71335-1922-0)
71335-1922-1 71335-1922 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20210811 N/A ANDA ANDA203974 Bryant Ranch Prepack METRONIDAZOLE 500 mg/1 20 TABLET in 1 BOTTLE (71335-1922-1)
71335-1922-2 71335-1922 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20210826 N/A ANDA ANDA203974 Bryant Ranch Prepack METRONIDAZOLE 500 mg/1 30 TABLET in 1 BOTTLE (71335-1922-2)
71335-1922-3 71335-1922 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20211007 N/A ANDA ANDA203974 Bryant Ranch Prepack METRONIDAZOLE 500 mg/1 14 TABLET in 1 BOTTLE (71335-1922-3)
71335-1922-4 71335-1922 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20241031 N/A ANDA ANDA203974 Bryant Ranch Prepack METRONIDAZOLE 500 mg/1 56 TABLET in 1 BOTTLE (71335-1922-4)
71335-1922-5 71335-1922 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20211209 N/A ANDA ANDA203974 Bryant Ranch Prepack METRONIDAZOLE 500 mg/1 21 TABLET in 1 BOTTLE (71335-1922-5)
71335-1922-6 71335-1922 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20211004 N/A ANDA ANDA203974 Bryant Ranch Prepack METRONIDAZOLE 500 mg/1 4 TABLET in 1 BOTTLE (71335-1922-6)
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