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=ANDA070772"
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
71335-2949-1 71335-2949 HUMAN PRESCRIPTION DRUG metronidazole metronidazole TABLET ORAL 20251030 N/A ANDA ANDA070772 Bryant Ranch Prepack METRONIDAZOLE 125 mg/1 56 TABLET in 1 BOTTLE (71335-2949-1)
72162-2468-2 72162-2468 HUMAN PRESCRIPTION DRUG metronidazole metronidazole TABLET ORAL 20250327 N/A ANDA ANDA070772 Bryant Ranch Prepack METRONIDAZOLE 125 mg/1 56 TABLET in 1 BOTTLE (72162-2468-2)
72162-2468-5 72162-2468 HUMAN PRESCRIPTION DRUG metronidazole metronidazole TABLET ORAL 20250428 N/A ANDA ANDA070772 Bryant Ranch Prepack METRONIDAZOLE 125 mg/1 500 TABLET in 1 BOTTLE (72162-2468-5)
60687-526-01 60687-526 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20200409 N/A ANDA ANDA070772 American Health Packaging METRONIDAZOLE 250 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-526-01) / 1 TABLET in 1 BLISTER PACK (60687-526-11)
60687-550-01 60687-550 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET ORAL 20200320 N/A ANDA ANDA070772 American Health Packaging METRONIDAZOLE 500 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-550-01) / 1 TABLET in 1 BLISTER PACK (60687-550-11)
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