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=ANDA090222"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
46708-021-71 46708-021 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20100507 N/A ANDA ANDA090222 Alembic Pharmaceuticals Limited METRONIDAZOLE 750 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-021-71)
46708-021-30 46708-021 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20100507 N/A ANDA ANDA090222 Alembic Pharmaceuticals Limited METRONIDAZOLE 750 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-021-30)
46708-021-31 46708-021 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20100507 N/A ANDA ANDA090222 Alembic Pharmaceuticals Limited METRONIDAZOLE 750 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-021-31)
46708-021-50 46708-021 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED, EXTENDED RELEASE ORAL 20100507 N/A ANDA ANDA090222 Alembic Pharmaceuticals Limited METRONIDAZOLE 750 mg/1 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-021-50)
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