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
70518-2305-4	70518-2305	HUMAN PRESCRIPTION DRUG	Metronidazole	Metronidazole	TABLET, FILM COATED	ORAL	20250913	N/A	ANDA	ANDA203458	REMEDYREPACK INC.	METRONIDAZOLE	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2305-4)
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)
70518-1536-3	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)
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)