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
29300-296-01	29300-296	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230715	N/A	ANDA	ANDA213083	Unichem Pharmaceuticals (USA), Inc.	RANOLAZINE	500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29300-296-01)
29300-296-05	29300-296	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230715	N/A	ANDA	ANDA213083	Unichem Pharmaceuticals (USA), Inc.	RANOLAZINE	500 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29300-296-05)
29300-296-16	29300-296	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230715	N/A	ANDA	ANDA213083	Unichem Pharmaceuticals (USA), Inc.	RANOLAZINE	500 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29300-296-16)
29300-297-01	29300-297	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230715	N/A	ANDA	ANDA213083	Unichem Pharmaceuticals (USA), Inc.	RANOLAZINE	1000 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29300-297-01)
29300-297-16	29300-297	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230715	N/A	ANDA	ANDA213083	Unichem Pharmaceuticals (USA), Inc.	RANOLAZINE	1000 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29300-297-16)
29300-297-52	29300-297	HUMAN PRESCRIPTION DRUG	Ranolazine	Ranolazine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230715	N/A	ANDA	ANDA213083	Unichem Pharmaceuticals (USA), Inc.	RANOLAZINE	1000 mg/1	250 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29300-297-52)