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=ANDA203458"
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
43063-719-06 43063-719 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20161102 N/A ANDA ANDA203458 PD-Rx Pharmaceuticals, Inc. METRONIDAZOLE 250 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-719-06)
43063-719-21 43063-719 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20170501 N/A ANDA ANDA203458 PD-Rx Pharmaceuticals, Inc. METRONIDAZOLE 250 mg/1 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-719-21)
43063-719-28 43063-719 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20170503 N/A ANDA ANDA203458 PD-Rx Pharmaceuticals, Inc. METRONIDAZOLE 250 mg/1 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-719-28)
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