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=ANDA076796"
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
43063-849-30 43063-849 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20180427 N/A ANDA ANDA076796 PD-Rx Pharmaceuticals, Inc. FUROSEMIDE 20 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (43063-849-30)
43063-849-60 43063-849 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20180503 N/A ANDA ANDA076796 PD-Rx Pharmaceuticals, Inc. FUROSEMIDE 20 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (43063-849-60)
43063-849-90 43063-849 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20180503 N/A ANDA ANDA076796 PD-Rx Pharmaceuticals, Inc. FUROSEMIDE 20 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (43063-849-90)
72162-1362-5 72162-1362 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20240202 N/A ANDA ANDA076796 Bryant Ranch Prepack FUROSEMIDE 80 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (72162-1362-5)
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