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
59651-297-01	59651-297	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, EXTENDED RELEASE	ORAL	20210719	N/A	ANDA	ANDA213361	Aurobindo Pharma Limited	NIFEDIPINE	90 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-297-01)
59651-295-01	59651-295	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, EXTENDED RELEASE	ORAL	20210719	N/A	ANDA	ANDA213361	Aurobindo Pharma Limited	NIFEDIPINE	30 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-295-01)
72162-2535-1	72162-2535	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, EXTENDED RELEASE	ORAL	20250919	N/A	ANDA	ANDA213361	Bryant Ranch Prepack	NIFEDIPINE	60 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2535-1)
68071-2838-3	68071-2838	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, EXTENDED RELEASE	ORAL	20221208	N/A	ANDA	ANDA213361	NuCare Pharmaceuticals,Inc.	NIFEDIPINE	30 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-2838-3)
59651-296-01	59651-296	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, EXTENDED RELEASE	ORAL	20210719	N/A	ANDA	ANDA213361	Aurobindo Pharma Limited	NIFEDIPINE	60 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-296-01)
72162-2536-1	72162-2536	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, EXTENDED RELEASE	ORAL	20250919	N/A	ANDA	ANDA213361	Bryant Ranch Prepack	NIFEDIPINE	90 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2536-1)
72162-2534-1	72162-2534	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, EXTENDED RELEASE	ORAL	20250919	N/A	ANDA	ANDA213361	Bryant Ranch Prepack	NIFEDIPINE	30 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2534-1)
67296-2170-1	67296-2170	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, EXTENDED RELEASE	ORAL	20210719	N/A	ANDA	ANDA213361	Redpharm Drug	NIFEDIPINE	30 mg/1	14 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-2170-1)