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
68382-689-01	68382-689	HUMAN PRESCRIPTION DRUG	NIFEDIPINE	NIFEDIPINE	TABLET, EXTENDED RELEASE	ORAL	20180818	N/A	ANDA	ANDA210184	Zydus Pharmaceuticals (USA) Inc.	NIFEDIPINE	60 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-689-01)
68382-689-10	68382-689	HUMAN PRESCRIPTION DRUG	NIFEDIPINE	NIFEDIPINE	TABLET, EXTENDED RELEASE	ORAL	20180818	N/A	ANDA	ANDA210184	Zydus Pharmaceuticals (USA) Inc.	NIFEDIPINE	60 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-689-10)
68382-689-16	68382-689	HUMAN PRESCRIPTION DRUG	NIFEDIPINE	NIFEDIPINE	TABLET, EXTENDED RELEASE	ORAL	20180818	N/A	ANDA	ANDA210184	Zydus Pharmaceuticals (USA) Inc.	NIFEDIPINE	60 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-689-16)
68382-689-77	68382-689	HUMAN PRESCRIPTION DRUG	NIFEDIPINE	NIFEDIPINE	TABLET, EXTENDED RELEASE	ORAL	20180818	N/A	ANDA	ANDA210184	Zydus Pharmaceuticals (USA) Inc.	NIFEDIPINE	60 mg/1	10 BLISTER PACK in 1 CARTON (68382-689-77) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
68382-688-10	68382-688	HUMAN PRESCRIPTION DRUG	NIFEDIPINE	NIFEDIPINE	TABLET, EXTENDED RELEASE	ORAL	20180818	N/A	ANDA	ANDA210184	Zydus Pharmaceuticals (USA) Inc.	NIFEDIPINE	30 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-688-10)
68382-688-16	68382-688	HUMAN PRESCRIPTION DRUG	NIFEDIPINE	NIFEDIPINE	TABLET, EXTENDED RELEASE	ORAL	20180818	N/A	ANDA	ANDA210184	Zydus Pharmaceuticals (USA) Inc.	NIFEDIPINE	30 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-688-16)
68382-689-95	68382-689	HUMAN PRESCRIPTION DRUG	NIFEDIPINE	NIFEDIPINE	TABLET, EXTENDED RELEASE	ORAL	20180818	N/A	ANDA	ANDA210184	Zydus Pharmaceuticals (USA) Inc.	NIFEDIPINE	60 mg/1	300 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-689-95)
68382-690-77	68382-690	HUMAN PRESCRIPTION DRUG	NIFEDIPINE	NIFEDIPINE	TABLET, EXTENDED RELEASE	ORAL	20180818	N/A	ANDA	ANDA210184	Zydus Pharmaceuticals (USA) Inc.	NIFEDIPINE	90 mg/1	10 BLISTER PACK in 1 CARTON (68382-690-77) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
68382-690-95	68382-690	HUMAN PRESCRIPTION DRUG	NIFEDIPINE	NIFEDIPINE	TABLET, EXTENDED RELEASE	ORAL	20180818	N/A	ANDA	ANDA210184	Zydus Pharmaceuticals (USA) Inc.	NIFEDIPINE	90 mg/1	300 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-690-95)
68382-690-01	68382-690	HUMAN PRESCRIPTION DRUG	NIFEDIPINE	NIFEDIPINE	TABLET, EXTENDED RELEASE	ORAL	20180818	N/A	ANDA	ANDA210184	Zydus Pharmaceuticals (USA) Inc.	NIFEDIPINE	90 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-690-01)
68382-690-10	68382-690	HUMAN PRESCRIPTION DRUG	NIFEDIPINE	NIFEDIPINE	TABLET, EXTENDED RELEASE	ORAL	20180818	N/A	ANDA	ANDA210184	Zydus Pharmaceuticals (USA) Inc.	NIFEDIPINE	90 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-690-10)
68382-690-16	68382-690	HUMAN PRESCRIPTION DRUG	NIFEDIPINE	NIFEDIPINE	TABLET, EXTENDED RELEASE	ORAL	20180818	N/A	ANDA	ANDA210184	Zydus Pharmaceuticals (USA) Inc.	NIFEDIPINE	90 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-690-16)