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）

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
54348-740-28	54348-740	HUMAN PRESCRIPTION DRUG	Metronidazole	METRONIDAZOLE	TABLET, FILM COATED	ORAL	20190710	N/A	ANDA	ANDA203458	PharmPak, Inc.	METRONIDAZOLE	500 mg/1	1 BOTTLE in 1 BOX (54348-740-28) / 28 TABLET, FILM COATED in 1 BOTTLE
68788-8674-1	68788-8674	HUMAN PRESCRIPTION DRUG	Metronidazole	Metronidazole	TABLET, FILM COATED	ORAL	20240523	N/A	ANDA	ANDA203458	Preferred Pharmaceuticals Inc.	METRONIDAZOLE	500 mg/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8674-1)
68788-8674-2	68788-8674	HUMAN PRESCRIPTION DRUG	Metronidazole	Metronidazole	TABLET, FILM COATED	ORAL	20240523	N/A	ANDA	ANDA203458	Preferred Pharmaceuticals Inc.	METRONIDAZOLE	500 mg/1	21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8674-2)
68788-8674-3	68788-8674	HUMAN PRESCRIPTION DRUG	Metronidazole	Metronidazole	TABLET, FILM COATED	ORAL	20240523	N/A	ANDA	ANDA203458	Preferred Pharmaceuticals Inc.	METRONIDAZOLE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8674-3)
55700-298-04	55700-298	HUMAN PRESCRIPTION DRUG	Metronidazole	Metronidazole	TABLET, FILM COATED	ORAL	20150921	20270331	ANDA	ANDA203458	Quality Care Products LLC	METRONIDAZOLE	500 mg/1	4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55700-298-04)
55700-298-14	55700-298	HUMAN PRESCRIPTION DRUG	Metronidazole	Metronidazole	TABLET, FILM COATED	ORAL	20150921	20270331	ANDA	ANDA203458	Quality Care Products LLC	METRONIDAZOLE	500 mg/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55700-298-14)
55700-298-21	55700-298	HUMAN PRESCRIPTION DRUG	Metronidazole	Metronidazole	TABLET, FILM COATED	ORAL	20150921	20270331	ANDA	ANDA203458	Quality Care Products LLC	METRONIDAZOLE	500 mg/1	21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55700-298-21)