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
64980-427-12	64980-427	HUMAN PRESCRIPTION DRUG	Tindazole	Tinidazole	TABLET, FILM COATED	ORAL	20131009	N/A	ANDA	ANDA202489	Rising Pharma Holdings, Inc.	TINIDAZOLE	500 mg/1	12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64980-427-12)
67296-1836-8	67296-1836	HUMAN PRESCRIPTION DRUG	Tindazole	Tinidazole	TABLET, FILM COATED	ORAL	20131009	N/A	ANDA	ANDA202489	Redpharm Drug, Inc.	TINIDAZOLE	500 mg/1	8 TABLET, FILM COATED in 1 BOTTLE (67296-1836-8)
64980-426-02	64980-426	HUMAN PRESCRIPTION DRUG	Tindazole	Tinidazole	TABLET, FILM COATED	ORAL	20131009	N/A	ANDA	ANDA202489	Rising Pharma Holdings, Inc.	TINIDAZOLE	250 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64980-426-02)
70518-4172-0	70518-4172	HUMAN PRESCRIPTION DRUG	Tindazole	Tinidazole	TABLET, FILM COATED	ORAL	20240830	N/A	ANDA	ANDA202489	REMEDYREPACK INC.	TINIDAZOLE	500 mg/1	8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4172-0)
70518-4172-1	70518-4172	HUMAN PRESCRIPTION DRUG	Tindazole	Tinidazole	TABLET, FILM COATED	ORAL	20240830	N/A	ANDA	ANDA202489	REMEDYREPACK INC.	TINIDAZOLE	500 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4172-1)