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
29300-226-05 29300-226 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20140601 N/A ANDA ANDA203458 Unichem Pharmaceuticals (USA), Inc. METRONIDAZOLE 250 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-226-05)
67046-1269-3 67046-1269 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20241111 N/A ANDA ANDA203458 Coupler LLC METRONIDAZOLE 250 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1269-3)
29300-226-10 29300-226 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20140601 N/A ANDA ANDA203458 Unichem Pharmaceuticals (USA), Inc. METRONIDAZOLE 250 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-226-10)
29300-226-46 29300-226 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20140601 N/A ANDA ANDA203458 Unichem Pharmaceuticals (USA), Inc. METRONIDAZOLE 250 mg/1 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-226-46)
29300-227-46 29300-227 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20140601 N/A ANDA ANDA203458 Unichem Pharmaceuticals (USA), Inc. METRONIDAZOLE 500 mg/1 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-227-46)
61919-032-14 61919-032 HUMAN PRESCRIPTION DRUG METRONIDAZOLE METRONIDAZOLE TABLET, FILM COATED ORAL 20170214 N/A ANDA ANDA203458 DIRECT RX METRONIDAZOLE 500 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (61919-032-14)
68001-364-00 68001-364 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20180801 N/A ANDA ANDA203458 BluePoint Laboratories METRONIDAZOLE 250 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68001-364-00)
68001-365-00 68001-365 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20180801 N/A ANDA ANDA203458 BluePoint Laboratories METRONIDAZOLE 500 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68001-365-00)
68001-365-03 68001-365 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20180801 N/A ANDA ANDA203458 BluePoint Laboratories METRONIDAZOLE 500 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68001-365-03)
70518-0058-0 70518-0058 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20161213 N/A ANDA ANDA203458 REMEDYREPACK INC. METRONIDAZOLE 500 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (70518-0058-0)
70518-0058-1 70518-0058 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20170110 N/A ANDA ANDA203458 REMEDYREPACK INC. METRONIDAZOLE 500 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (70518-0058-1)
70518-0088-0 70518-0088 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20161228 N/A ANDA ANDA203458 REMEDYREPACK INC. METRONIDAZOLE 500 mg/1 14 TABLET, FILM COATED in 1 BLISTER PACK (70518-0088-0)
70518-0088-2 70518-0088 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20161230 N/A ANDA ANDA203458 REMEDYREPACK INC. METRONIDAZOLE 500 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (70518-0088-2)
70518-0088-3 70518-0088 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20161230 N/A ANDA ANDA203458 REMEDYREPACK INC. METRONIDAZOLE 500 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (70518-0088-3)
70518-0088-4 70518-0088 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20170131 N/A ANDA ANDA203458 REMEDYREPACK INC. METRONIDAZOLE 500 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0088-4)
70518-0088-5 70518-0088 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20190513 N/A ANDA ANDA203458 REMEDYREPACK INC. METRONIDAZOLE 500 mg/1 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0088-5)
70518-1536-2 70518-1536 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20240516 N/A ANDA ANDA203458 REMEDYREPACK INC. METRONIDAZOLE 250 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1536-2)
70518-1536-3 70518-1536 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20250530 N/A ANDA ANDA203458 REMEDYREPACK INC. METRONIDAZOLE 250 mg/1 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1536-3)
71335-0358-0 71335-0358 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20181107 N/A ANDA ANDA203458 Bryant Ranch Prepack METRONIDAZOLE 500 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (71335-0358-0)
71335-0358-1 71335-0358 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20180227 N/A ANDA ANDA203458 Bryant Ranch Prepack METRONIDAZOLE 500 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-0358-1)
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