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=ANDA206560"
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
82868-014-30 82868-014 HUMAN PRESCRIPTION DRUG metronidazole metronidazole TABLET ORAL 20231130 N/A ANDA ANDA206560 Northwind Pharmaceuticals, LLC METRONIDAZOLE 500 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (82868-014-30)
70518-3042-2 70518-3042 HUMAN PRESCRIPTION DRUG metronidazole metronidazole TABLET ORAL 20221205 N/A ANDA ANDA206560 REMEDYREPACK INC. METRONIDAZOLE 250 mg/1 28 TABLET in 1 BLISTER PACK (70518-3042-2)
72789-195-06 72789-195 HUMAN PRESCRIPTION DRUG metronidazole metronidazole TABLET ORAL 20211029 N/A ANDA ANDA206560 PD-Rx Pharmaceuticals, Inc. METRONIDAZOLE 250 mg/1 6 TABLET in 1 BOTTLE, PLASTIC (72789-195-06)
72789-195-21 72789-195 HUMAN PRESCRIPTION DRUG metronidazole metronidazole TABLET ORAL 20210630 N/A ANDA ANDA206560 PD-Rx Pharmaceuticals, Inc. METRONIDAZOLE 250 mg/1 21 TABLET in 1 BOTTLE, PLASTIC (72789-195-21)
72789-195-30 72789-195 HUMAN PRESCRIPTION DRUG metronidazole metronidazole TABLET ORAL 20210630 N/A ANDA ANDA206560 PD-Rx Pharmaceuticals, Inc. METRONIDAZOLE 250 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (72789-195-30)
82982-039-14 82982-039 HUMAN PRESCRIPTION DRUG metronidazole metronidazole TABLET ORAL 20230315 20240731 ANDA ANDA206560 Pharmasource Meds, LLC METRONIDAZOLE 500 mg/1 14 TABLET in 1 BOTTLE (82982-039-14)
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