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
72789-485-01	72789-485	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, EXTENDED RELEASE	ORAL	20250212	N/A	ANDA	ANDA216067	PD-Rx Pharmaceuticals, Inc.	NIFEDIPINE	60 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-485-01)
72789-485-87	72789-485	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, EXTENDED RELEASE	ORAL	20250210	N/A	ANDA	ANDA216067	PD-Rx Pharmaceuticals, Inc.	NIFEDIPINE	60 mg/1	300 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-485-87)
72789-486-01	72789-486	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, EXTENDED RELEASE	ORAL	20250212	N/A	ANDA	ANDA216067	PD-Rx Pharmaceuticals, Inc.	NIFEDIPINE	90 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-486-01)
67296-2157-1	67296-2157	HUMAN PRESCRIPTION DRUG	Nifedipine	Nifedipine	TABLET, EXTENDED RELEASE	ORAL	20220330	N/A	ANDA	ANDA216067	Redpharm Drug	NIFEDIPINE	30 mg/1	10 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-2157-1)